ASSET PURCHASE AGREEMENT

Exhibit 2.1

EXECUTION

The Asset Purchase Agreement contains representations and warranties by the parties thereto. A party’s representations and warranties were made solely for the benefit of the other party or parties and (i) were not intended to be treated as categorical statements of fact, but rather as a way of allocating the risk to the party or parties making the representation and warranty if it proves to be inaccurate; (ii) may have been qualified in the Asset Purchase Agreement by disclosures that were made to the other party or parties in connection with the negotiation of the Asset Purchase Agreement (provided that any specific facts that contradict the representations and warranties in the Asset Purchase Agreement in any material respect have been disclosed); (iii) may apply contract standards of “materiality” that are different from “materiality” under the applicable securities laws; and (iv) were made only as of the date of the Asset Purchase Agreement or such other date or dates as may be specified in the Asset Purchase Agreement.

This Asset Purchase Agreement (this “Agreement”) is entered into March 7, 2012 by and among Vansen Pharma, Inc. 0000-0000 xxxx. Xx Xxxxxxxxxxx X., Xxxxxxxxx, Xxxxxx, XXXXXX, X0X 0X0 (“Purchaser”), and Cornerstone Therapeutics, Inc., a Delaware Corporation, with place of business at 0000 Xxxxxxxx Xxxxx Xxxxx, Xxxxx 000, Xxxx, XX00000 (“Seller”).

RECITALS

WHEREAS, Seller is the owner of certain assets described in Article II below (the “Purchased Assets”), related to the products described on Exhibit A (the “Products”);

WHEREAS, the Parties desire that, at the Closing, Purchaser shall purchase from Seller all of the Purchased Assets and assume all of the Assumed Liabilities upon the following terms and conditions:

NOW, THEREFORE, the Parties hereby agree as follows:

Article I.

Definitions and Terms

1.1 Definitions. The following terms are used in more than one Article of this Agreement and have the following meanings. Other defined terms may occur in one Article only and are defined therein:

“Affiliate” shall mean, with respect to any Person, any other Person directly or indirectly controlling, controlled by, or under common control with such Person at any time during the period for which the determination of affiliation is being made. For purposes of this definition, “control” of a Person means the power, direct or indirect, to direct or cause the direction of the management and policies of such Person whether by contract or otherwise and, in any event and without limitation of the previous sentence, ownership of more than fifty percent (50%) of the voting securities of such Person.

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Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

“Ancillary Agreements” shall mean the Assignment and Assumption Agreement, the Xxxx of Sale, the Co-Promotion Agreement, the License Assignment, and the Transition Services Agreement.

“Assignment and Assumption Agreement” shall mean the Assignment and Assumption Agreement in the form attached as Exhibit B to this Agreement, providing for the assignment of the Assumed Contracts and Seller’s rights under purchase orders that are not fully satisfied prior to Closing.

“Assumed Contracts” shall mean the Transferred License and the other contracts set forth on Schedule 2.1(a).

“Assumed Liabilities” shall have the meaning set forth in Section 2.3.

“Xxxx of Sale” shall mean the Xxxx of Sale in the form attached as Exhibit C to this Agreement.

“Books and Records” shall mean all files, documents, books, records, lists, procedures, manuals and other materials (in any form), regardless of whether created by Seller, acquired from third parties, maintained in Seller’s possession or control, including financial and accounting records; catalogues; competitive intelligence, advertising, detail aids, sales and promotional and marketing materials; training and educational materials; market research; business plans; price lists; correspondence; customer, mailing and distribution lists; referral sources; photographs; customer lists, supplier lists; call data; call notes; prosecution history, records and related files; purchasing materials and records; clinical data files; formulae and specifications used for design, manufacture, packaging and labeling; manufacturing, cGMP and quality control records and procedures (including batch records and batch samples); production data; process validation reports; stability data; blueprints; research and development files, records, data and laboratory books; the dossiers supporting any Product Registrations; other regulatory, medical affairs and pharmacovigilance records, including adverse event documentation and complaint documentation; intellectual property documentation and disclosures; service and warranty records; sales order files; website and other Internet content.

“Business Day” shall mean any day other than a Saturday, a Sunday or a day on which banks in New York City, New York are authorized or obligated by Law or Governmental Order to close.

“Closing” shall mean the consummation of the transactions contemplated by this Agreement pursuant to the terms of this Agreement.

“Closing Date” shall have the meaning set forth in Section 3.1.

“Co-Promotion Agreement” shall mean the Co-Promotion Agreement executed by the parties as of the Closing date and attached as Exhibit D.

“Confidential Disclosure Agreement” shall mean that certain confidential disclosure agreement effective as of February 10, 2012 between Purchaser and Seller.

“GAAP” shall mean accounting principles generally accepted in the United States, as in effect from time to time.

“Governmental Authority” shall mean any supranational, national, federal, provincial, state or local judicial, legislative, executive, administrative or regulatory authority, board, commission, body or instrumentality.

“Governmental Authorization” shall mean any approval, certificate, clearance, consent, exemption, governmental order, license, permit, registration, variance or other authorization issued, granted, given or otherwise made available by or under the authority of any Governmental Authority or pursuant to any applicable Law.

“Inventories” shall mean all inventories of active pharmaceutical ingredient, work in progress and finished goods of each Product owned as of the Closing by Seller, and shall include any samples.

“Law” shall mean any national, federal, territorial, state, provincial, regional, foreign, municipal or local law (including common law and civil law), statute, ordinance, rule, regulation, code, treaty, decree, ruling, directive or order, in each case, of, or issued by, any Governmental Authority.

“Liabilities” shall mean any and all debts, liabilities, costs, assessments, expenses, claims, losses, damages, deficiencies and obligations, whether accrued or fixed, known or unknown, liquidated or unliquidated, asserted or unasserted, absolute or contingent, matured or unmatured, determined or determinable, due or to become due, whenever or however arising (including whether arising out of any contract, common law or tort based on negligence or strict liability) and whether or not the same would be required by GAAP to be reflected in financial statements or disclosed in the notes thereto.

“License Agreement Assignment” shall mean the Assignment of the Transferred License in the form attached as Exhibit E to this Agreement.

“Lien” shall mean, with respect to any property, right or other asset, any lien, security interest, option, mortgage, pledge, condition, assessment, restriction, adverse claim, levy, charge, hypothecation, easement, title retention clause, equitable interest, encumbrance, right of first refusal or other restriction or similar claim of any kind, character or description, whether or not of record, or any contract to give any of the foregoing, in respect of such property or asset.

“Material Adverse Effect” shall mean any change, effect, event, circumstance, occurrence or state of facts that, individually or in the aggregate, is or would reasonably be expected to be materially adverse to (i) the Purchased Assets taken as a whole or (ii) the ability of Seller to consummate the transactions contemplated by this Agreement and the Ancillary Agreements; provided, however, that none of the following changes, effects, events, circumstances, occurrences or states of facts shall be deemed, either alone or in combination,

to constitute a Material Adverse Effect, or be taken into account in determining whether a Material Adverse Effect has occurred or would reasonably be expected to occur: (A) changes or effects in general economic or financial conditions; (B) changes in Laws or GAAP; (C) changes or effects that generally affect the pharmaceutical industry; or (D) changes or effects that arise out of or are attributable to the commencement, occurrence, continuation or intensification of any war, sabotage, armed hostilities or acts of terrorism.

“Party” shall mean Purchaser or Seller individually, as the context so requires, and the term “Parties” shall mean, collectively, Seller and Purchaser.

“Person” shall mean an individual, a limited liability company, a joint venture, a corporation, a partnership, an association, a Governmental Authority, a trust or any other entity or organization.

“Product” or “Products” shall mean those products set out on Exhibit A.

“Product Liability” shall mean liability resulting from a claim by any individual or Governmental Authority that a Product has caused or is likely to cause injury or damage as a result of its being defective or inherently dangerous.

“Product Registrations” shall mean the Governmental Authorizations necessary to permit the development, manufacture, marketing, import, distribution, or sale of the Products.

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“Purchased Assets” shall have the meaning set forth in Section 2.1.

“Regulatory Fees” shall mean all the regulatory fees paid by Seller to the FDA with respect to the federal fiscal year beginning October 1, 2011 in connection with the manufacture of the Products and set out in Section 5.15(f) of the Seller Disclosure Letter.

“Representatives” shall mean, with respect to each Party, its and its Affiliates’ respective parents, directors, officers, employees, attorneys, accountants, representatives, financial advisors, consultants, agents and others acting on their behalf.

“Retained Liabilities” shall have the meaning set forth in Section 2.4.

“Seller Disclosure Letter” shall mean the written disclosure letter delivered separately by Seller to Purchaser concurrently with the execution and delivery of this Agreement.

“Seller Names” shall mean the names, logos and trademarks of Seller and its Affiliates used with respect to the Products by Seller and its Affiliates prior to the Closing.

“Seller’s Knowledge” shall mean the actual knowledge of each of the persons listed as Named Executive Officers in Seller’s 2011 Proxy Statement filed with the Securities and Exchange Commission on Form 14A, after due inquiry.

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Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

“Taxes” shall mean all taxes, charges, duties, fees, levies or other assessments, including income, excise, property, ad valorem, sales or use, value added, profits, license, withholding (with respect to compensation or otherwise), payroll, employment, net worth, capital gains, transfer, stamp, social security, environmental, occupation and franchise taxes, imposed by any Taxing Authority, and including any interest, penalties and additions attributable thereto, and all amounts payable pursuant to an agreement or arrangement with respect to taxes.

“Taxing Authority” shall mean any Governmental Authority exercising any authority to impose, regulate or administer the imposition of Taxes.

“Transferred License” shall mean that certain License and Supply Agreement effective 10/12/2006 by and between Meiji Seika Kaisha, Ltd. and Cornerstone Biopharma, Inc., as amended by Amendment No. 1 effective 07/27/2007, Letter Agreement dated 07/27/2007, Letter Agreement dated 01/11/2008 and Addendum effective 08/14/2008.

“Transition Services Agreement” shall mean the Transition Services Agreement executed by the parties as of the Closing date and attached as Exhibit D.

Article II.

Purchase and Sale

2.1 Purchase and Sale of Assets. At the Closing, Purchaser shall purchase and acquire from Seller, free and clear of all Liens, all of Seller’s right, title and interest in and to the following assets (the “Purchased Assets”):

(a) the Assumed Contracts;

(b) the Books and Records;

(d) the Product Registrations; and

(e) all rights under purchase orders that are not fully satisfied prior to Closing.

2.2 Excluded Assets. Purchaser acknowledges and agrees that it is not acquiring any right, title or interest in, to or under any other assets, properties or rights of Seller or any of its Affiliates other than the Purchased Assets.

2.3 Assumed Liabilities. Purchaser agrees, effective at the Closing, to assume the following:

(a) all Liabilities to customers, suppliers or other third parties based solely on acts relating to the Purchased Assets arising or incurred after the Closing Date;

(b) all Liabilities, including product liabilities, arising out of or relating to any sale of the Product sold by Purchaser, an Affiliate of Purchaser, or a third party directed by Purchaser after the Closing Date;

(c) all Liabilities relating solely to the return of any Product, without regard to when such Product was sold, provided, however, that Purchaser shall not be responsible for any Product Liability related to or arising out of the distribution, including but not limited to sales, of Product prior to the Closing Date;

(d) all Liabilities arising out of or related to the Assumed Contracts for acts occurring after the Closing Date;

(e) all Taxes relating to a taxable period beginning after the Closing Date including, with respect to any taxable period beginning before and ending after the Closing Date, the portion of such taxable period beginning after the Closing Date; and

(f) all Regulatory Fees relating to any period after the Closing Date.

2.4 Retained Liabilities. Except as set forth in Section 2.3, Seller shall retain and, as between Seller and Purchaser, be solely responsible for all Liabilities, including product liabilities, to all parties, including customers, suppliers or other third parties, relating to any sale or disposal of the Product before the Closing Date or relating to the Purchased Assets arising or incurred before the Closing Date, and all Liabilities to the extent such Liabilities are attributable to Seller’s breaches or defaults under an Assumed Contract that occurred prior to the Closing Date.

2.5 Purchase Price. In consideration of the sale and transfer of the Purchased Assets, Purchaser shall:

(a) pay to Seller at the Closing an amount (the “Closing Purchase Price”) equal to the [***], such amount to be paid by wire transfer of immediately available funds in accordance with written instructions given to Purchaser by Seller. Seller agrees that the samples included in Inventory on Schedule 2.6 of this Agreement will be listed as zero cost to Purchaser. To be clear, Seller agrees to provide all samples remaining in Inventory at no cost to Purchaser; and

(b) pay to the Seller [***] in five equal monthly installments beginning May 15, 2012 and to be invoiced on a monthly basis.

2.6 Purchase Price Adjustment.

(a) At least two (2) Business Days prior to the Closing Date, Seller shall deliver to Purchaser (i) a good faith estimate of the Inventories as of the Closing that have forward dating of a minimum of fifteen (15) months (the “Estimated Inventories”), valued according to the calculation methodology set out on Schedule 2.6. The Estimated Inventories shall be paid at the Closing.

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Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

(b) Within forty-five (45) days after the Closing Date, Purchaser shall deliver to Seller an unaudited statement of the Inventories delivered, and the resulting value calculated in accordance with Schedule 2.6 (the “Closing Date Inventories” and the “Inventories Statement”)

(c) During the thirty (30) day period following Seller’s receipt of the Inventories Statement, Seller shall be given access to the employees, working papers and other Books and Records of Purchaser for purposes of evaluating the Inventories Statement. Seller may notify Purchaser in writing of any disputed item within thirty (30) days after receipt of the Inventories Statement.

(d) If a notice of disputed items is timely delivered, Seller and Purchaser shall, during the thirty (30) day period immediately following the date of such delivery negotiate to resolve the disputed items. If the Parties are unable to reach agreement during the thirty (30) day period with respect to any item, such dispute shall be resolved according to the dispute resolution provisions of this Agreement.

(e) If the Final Inventories are greater than the Estimated Inventories, Purchaser shall, within five (5) Business Days after the determination of the Final Inventories, pay to Seller, by wire transfer of immediately available funds in accordance with written instructions given by Seller to Purchaser, the amount of such excess. If the Final Inventories are less than the Estimated Inventories, Seller shall, within five (5) Business Days after the determination of the Final Inventories, pay to Purchaser, by wire transfer of immediately available funds in accordance with written instructions given by Purchaser to Seller, the amount of such shortfall.

(f) All payments made pursuant to this Section 2.6 shall be treated for Tax purposes as an adjustment to the Purchase Price, unless otherwise required by applicable Law.

2.7 Allocation of Purchase Price. The Parties agree that the Closing Purchase Price shall be allocated [***]. In the event that any Taxing Authority disputes the Parties allocation, each Party shall promptly notify the other Parties in writing of the nature of such dispute.

2.8 Taxes.

(a) United States Taxes - All transfer, documentary sales, use, value-added, gross receipts, stamp, registration or similar transfer Taxes incurred in connection with the transfer and sale of the Purchased Assets as contemplated by the terms of this Agreement, including all recording or filing fees and other similar costs of Closing that may be imposed, payable, collectible or incurred in connection with this Agreement and the transactions contemplated hereby and payable to any local, state or Federal tax agency of the United States shall be paid by Seller. Purchaser and Seller shall cooperate in timely making all Tax returns as may be required to comply with applicable Laws.

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Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

(b) Canada Taxes - All transfer, documentary sales, use, value-added, gross receipts, stamp, registration or similar transfer Taxes incurred in connection with the transfer and sale of the Purchased Assets as contemplated by the terms of this Agreement, including all recording or filing fees and other similar costs of Closing that may be imposed, payable, collectible or incurred in connection with this Agreement and the transactions contemplated hereby and payable to any local, Province, or Federal tax agency of Canada shall be paid by Purchaser. Purchaser and Seller shall cooperate in timely making all Tax returns as may be required to comply with applicable Laws.

(c) All personal property Taxes and assessments on the Purchased Assets for any taxable period commencing prior to the Closing Date and ending after the Closing Date shall be prorated on a per diem basis between Purchaser and Seller as of the Closing. The amount of all such prorations payable by the Party that is not required to pay such Tax under applicable Law shall be paid to the Party required to pay such Tax under applicable Law fifteen (15) days before the date such Tax becomes due and payable and such amount shall be timely remitted to the applicable Taxing Authority; provided, however, that if such Tax has already been paid to the Taxing Authority prior to the Closing Date, then such amounts shall be paid on the Closing Date to the Party required to pay such Taxes under applicable Law.

(d) Each Party shall cooperate and otherwise take commercially reasonable efforts to obtain appropriate exemptions for or refunds of such Transfer Taxes or property Taxes and to minimize any such Transfer Taxes or property Taxes.

2.9 Risk of Loss. Prior to the Closing, any loss or damage to the Purchased Assets from fire, casualty or otherwise shall be the sole responsibility of Seller. Thereafter, any such loss or damage shall be the sole responsibility of Purchaser.

2.10 Coupon Prefund Balance. Purchaser acknowledges that the amounts set out in Schedule 2.10 reflect cash balances of deposits and pre-paid amounts that were on hand with any provider of coupon related services related to the Products as of February 29, 2012 (the “Provisional Coupon Prefund Balance”). Within forty-five (45) days after the Closing Date, Purchaser shall deliver to Seller a statement of the actual cash balances that were on hand with any provider of coupon related services as of the Closing Date (the “Closing Coupon Prefund Balance”). On the date six months following the Closing Date, Purchaser shall pay to Seller an amount equal to the Closing Coupon Prefund Balance, by wire transfer of immediately available funds in accordance with written instructions given by Seller to Purchaser.

Article III.

Closing

3.1 Closing Date. The Closing shall take place at such time and place as the Parties may mutually agree but shall not be unreasonably delayed. The date on which the Closing occurs is referred to as the “Closing Date.”

3.2 Closing Deliverables.

(a) At the Closing, Seller shall deliver, or cause to be delivered, to Purchaser:

(i)

to the extent it is practicable to do so, physical possession of the Inventories; and

(ii)

an executed counterpart of each of the Ancillary Agreements.

(b) At the Closing, Purchaser shall deliver, or cause to be delivered, to Seller:

(i)

the Closing Purchase Price pursuant to Section 2.5; and

(ii)

an executed counterpart to each of the Ancillary Agreements;

Article IV.

Transfer of Product Registrations and Delivery of Books and Records

4.1 Notice to FDA. On the Closing Date, Seller shall deliver a letter or letters to the FDA transferring the rights to the Product Registrations to Purchaser (or its designate) and a letter or letters to the FDA, notifying it of the transfer of the Product Registrations to Purchaser (or its designate), as well as any similar letters to any other applicable Regulatory Agencies Governmental Authority. On the Closing Date, Purchaser shall deliver a letter or letters to the FDA assuming responsibility for the Product Registrations from Seller and a letter or letters to the FDA, notifying it of the transfer of the Product Registrations from Seller to Purchaser (or its designate), as well as any similar letters to any other applicable Regulatory Agencies. Notwithstanding any delay in transferring the rights to the Product Registrations to Purchaser (or its designate), as between the Parties, Purchaser shall be exclusively responsible for, and shall discharge all liabilities related to, the manufacture, packaging, labeling, promotion, handling or sale of the Products by or on behalf of Purchaser after the Closing.

4.2 Books and Records Delivery. As soon as practical after the Closing Date and in no event after the expiration of the Transition Services Agreement, Seller shall deliver to Purchaser (or its designate), in physical and electronic form, all Books and Records prepared in connection with, supporting or otherwise relating to the Product or Product Registrations, including all correspondence between Seller or any of its representatives and the applicable Governmental Authority, all currently approved or required packaging or labeling and any other existing files and dossiers, in each case to the extent relating to any Product Registration or to the underlying data or information used to support, maintain or obtain marketing authorization of the underlying Product.

4.3 Commercially Reasonable Efforts. Seller shall use all commercially reasonable efforts to complete the transfer of each Product Registration as promptly as practicable after the Closing. Purchaser and its Affiliates shall use all commercially reasonable efforts to assist Seller in the transfer of the Product Registrations, accept the transfer of the Product Registrations and formalize with Seller and any applicable Governmental Authority, as promptly as practicable after the Closing Date, all necessary documents. Following such transfer, Seller shall not retain any rights in any Product Registration.

Article V.

Representations and Warranties of Seller

Seller represents and warrants to Purchaser as follows:

5.1 Organization. Seller is a corporation duly organized, validly existing and in good standing under the Laws of the jurisdiction of its organization.

5.2 Authority. Seller has all requisite company or corporate power and authority to own and operate the Purchased Assets, to execute and deliver this Agreement and the Ancillary Agreements and to perform its obligations hereunder and thereunder. The execution and delivery by Seller of this Agreement and the Ancillary Agreements and the performance by Seller of its obligations hereunder and thereunder have been duly authorized by all requisite company or corporate action on the part of Seller.

5.3 Non-Contravention. As set forth on Schedule 5.3 of Seller’s Disclosure Letter, the execution and delivery of, and the performance of the actions contemplated by this Agreement and each Ancillary Agreement by Seller, will not violate any provision, conflict with, or result in the breach of any Assumed Contract, or result in a breach of any applicable Law.

5.4 Governmental Authorization. Seller has obtained all Governmental Authorizations required by or with respect to Seller or the Purchased Assets in connection with the execution and delivery of this Agreement or any Ancillary Agreement or the consummation of the transactions contemplated hereby and thereby.

5.5 Financial Information. The financial information set forth in Section 5.5 of the Seller Disclosure Letter fairly presents, in all material respects, for the periods indicated, the net sales and product contribution (each as described therein) of the Products in accordance with GAAP, consistently applied throughout the periods involved.

5.6 Absence of Material Changes. Since December 31, 2011, except as set forth in Section 5.6 of the Seller Disclosure Letter:

(a) there has not been any Material Adverse Effect; and

(b) Seller has not engaged in any activity that would reasonably be expected to result in sales that are materially in excess of normal customer purchasing patterns.

5.7 Legal Proceedings. There is no pending or, to the Seller’s Knowledge threatened, complaint, claim, action, suit, case, litigation, proceeding, charge, criminal prosecution, investigation, arbitration, mediation or alternative dispute resolution proceeding by or before a Governmental Authority relating to the Purchased Assets.

5.8 Compliance with Laws.

(a) Seller has been during the past three (3) years in compliance in all material respects with, and, to the Seller’s Knowledge, is not under investigation by a Governmental Authority with respect to any material violation of, any Law applicable to the Purchased Assets.

(b) All Product Registrations have been duly obtained and are in full force and effect, and Seller is in compliance in all material respects with each Product Registration held by it with respect to the Products.

5.9 Assumed Contracts.

(a) The Assumed Contracts are valid and binding agreements of Seller and are in full force and effect; to Seller’s Knowledge, no party thereto is in default or breach in any material respect under the terms of, or has provided any written notice of any intention to terminate or modify, any Assumed Contract.

(b) Seller has provided Purchaser a complete and accurate copy of each Assumed Contract, including all modifications and amendments thereto and waivers thereunder.

5.10 Intellectual Property.

(a) To the Seller’s Knowledge, Seller is the sole and exclusive licensee of all the intellectual property covered by the Transferred License. Except as set forth in Section 5.10 of the Seller Disclosure Letter, Seller has not granted any rights or licenses of any kind relating to any such intellectual property and has not itself challenged the validity of such intellectual property.

(b) To Seller’s Knowledge, except as set forth in Section 5.10 of the Seller Disclosure Letter, no third party is infringing any intellectual property covered by the Transferred License.

(c) To Seller’s Knowledge, the manufacture and sale of the Products does not infringe any intellectual property of any Person.

(d) To Seller’s Knowledge, Seller has all necessary rights to grant to Purchaser the rights to the Seller Names pursuant to Section 7.

5.11 Title to Purchased Assets. Seller owns the Purchased Assets free and clear of all Liens.

5.12 Inventories. All Inventories that are finished goods conform to all applicable specifications in, and, to Seller’s Knowledge, have been manufactured in compliance with, all applicable Governmental Authorizations.

5.13 Suppliers. There are no suppliers of Inventory other than those that are party to Assumed Contracts.

5.14 Tax Matters.

(a) Seller has paid on a timely basis all Taxes relating to the Purchased Assets that are due and payable. There are no Liens with respect to Taxes on any of the Purchased Assets, other than statutory Liens for current Taxes not yet due and payable.

(b) There are no pending or, to the Seller’s Knowledge, threatened audits, investigations, disputes, notices of deficiency, claims or other actions or proceedings for or relating to any Taxes of Seller which would reasonably be expected to result in any Liens on any Purchased Asset or result in any material liability of Purchaser for any Tax.

5.15 Regulatory Matters.

(a) Seller holds all Product Registrations required by any Governmental Authority and all such Product Registrations are valid and in full force and effect. There has not occurred any violation of, default (with or without notice or lapse of time or both) under, or event giving to any Governmental Authority any right of termination or cancellation of any Product

Registration. To Seller’s Knowledge, no event has occurred that would reasonably be expected to result in the revocation, cancellation, non-renewal or adverse modification of any Product Registration, except as would not be material with respect to the Products and the Purchased Assets.

(b) Seller has completed and filed all reports, documents, claims, permits and notices required by any Governmental Authority in order to maintain the Product Registrations. To Seller’s Knowledge, all such reports, documents, claims, permits and notices were complete and accurate in all material respects on the date filed (or were corrected in or supplemented by a subsequent filing). Neither Seller, nor to Seller’s Knowledge, any representative or distributor of Seller has been convicted of any crime or engaged in any conduct for which debarment is mandated by 21 U.S.C. § 335a(a) or authorized by 21 U.S.C. § 335a(b) or any similar Law.

(c) Seller has not voluntarily or involuntarily initiated or caused to be initiated any recall “dear doctor” letter relating to an alleged lack of safety, efficacy or regulatory compliance of any Product.

(d) Neither Seller nor, to Seller’s Knowledge, any other Person has received any written notice that any Governmental Authority has:

(i)

commenced, or threatened to initiate, any action to request the recall of any Product;

(ii)

commenced, or threatened to initiate, any action to enjoin manufacture or distribution of any Product; or

(iii)

issued any demand letter, finding of deficiency or non-compliance or adverse inspection report (including any FDA Form 483s, FDA Notices of Adverse Findings, Untitled Letters, or Warning Letters) in respect of any Product, except as would not be material with respect to the Products and the Purchased Assets.

(e) Except as set forth in Section 5.15(e) of the Seller Disclosure Letter, in the past three (3) years, no Seller or, to the Seller’s Knowledge, any other Person has received any warning letter from the FDA or any other Governmental Authority regarding inappropriate advertising or marketing of any Product or any written notice of any actual or potential violation of Law, except as would not, individually or in the aggregate, have a Material Adverse Effect.

(f) The Regulatory Fees were timely paid by Seller prior to the Closing Date with respect to the Products for the federal fiscal year ending September 30, 2012 and Section 5.15(f) of the Seller Disclosure Letter sets forth the basis for the calculation of such fees.

(g) In the past three (3) years, except as set forth in Section 5.15(g) of the Seller Disclosure Letter, there have been no material audits, inspections or, to the Seller’s Knowledge, investigations of records by a Governmental Authority (other than in respect of Taxes) relating to the Purchased Assets.

5.16 Brokers. No broker, finder or investment banker is entitled to any brokerage, finders or other fee or commission in connection with the transactions contemplated by this Agreement based upon arrangements made by or on behalf of Seller.

5.17 Personnel. All of the Personnel listed on Schedule 5.17 are employees in good standing with Seller. Seller has made available to Purchaser a schedule setting forth the compensation earned by each of the Personnel as of the date of Closing.

Article VI.

Representations and Warranties of Purchaser

Purchaser represents and warrants to Seller as follows:

6.1 Organization. Purchaser is a corporation duly organized, validly existing and in good standing under the Business Corporations Act of Quebec, Canada.

6.2 Authority; Binding Effect. Purchaser has all requisite corporate power and authority to own and operate its properties and assets, to execute and deliver this Agreement and the Ancillary Agreements and to perform its obligations hereunder and thereunder. The execution and delivery by Purchaser of this Agreement and the Ancillary Agreements and the performance by Purchaser of its obligations hereunder and thereunder have been duly authorized by all requisite corporate action on the part of Purchaser.

6.3 Non-Contravention. The execution and delivery of, and the performance of the actions contemplated by this Agreement and each Ancillary Agreement by Purchaser will not violate any applicable Law.

6.4 Governmental Authorization. Purchaser has obtained all Governmental Authorizations required by or with respect to Purchaser in connection with the execution and delivery of this Agreement or any Ancillary Agreement or the consummation of the transactions contemplated hereby and thereby.

6.5 Condition of the Purchased Assets. Purchaser is knowledgeable about the industry in which Seller conducts its business with respect to the Products. Purchaser acknowledges and agrees that (i) it is purchasing the Purchased Assets and assuming the Assumed Liabilities based on the results of its own independent investigations and the representations and warranties of Seller expressly set forth in this Agreement, and not on any representation or warranty of Seller or any of its Representatives not expressly set forth in this Agreement and (ii) except as otherwise set forth in this Agreement, the Purchased Assets are sold “as is, where is” and Purchaser accepts the Purchased Assets in the condition they are in and at the place where they are located on the Closing, subject to the terms and conditions hereof. In light of these investigations and the representations and warranties expressly made to Purchaser by Seller herein, Purchaser is relinquishing any right to any claim based on any representations and warranties other than those expressly set forth in this Agreement. Any claims Purchaser may have for breach of representation or warranty shall be based solely on the representations and warranties of Seller expressly set forth in this Agreement. ALL WARRANTIES OF MERCHANTABILITY AND FITNESS FOR ANY PARTICULAR PURPOSE, AND ALL OTHER WARRANTIES ARISING UNDER THE UNIFORM COMMERCIAL CODE (OR SIMILAR APPLICABLE FOREIGN LAWS), ARE HEREBY WAIVED BY PURCHASE

6.6 Brokers. A broker, finder or investment banker is entitled to a brokerage, finders or other fee or commission in connection with the transactions contemplated by this Agreement based upon arrangements made by or on behalf of Purchaser. Purchaser is responsible for any such fee or commission set forth in this subsection 6.6.

Article VII.

Covenants

7.1 Information and Documents.

(a) For so long as the Transition Services Agreement is in effect, upon reasonable advance notice in writing and to the extent permitted by applicable Law, Seller shall permit Purchaser and its Representatives to have reasonable access, during normal business hours, to the properties, assets, agreements, Books and Records and personnel of Seller relating to the Purchased Assets as may reasonably be requested by Purchaser.

(b) Purchaser and Seller will retain all Books and Records pertinent to the Purchased Assets relating to Tax matters until the expiration of the applicable period for assessment under applicable Laws (giving effect to any and all extensions or waivers), and, if relating to other than Tax matters, for the period specified under such retaining Party’s document retention policy or, if longer, the longest period specified under applicable Laws.

7.2 Trade Notification. Seller and Purchaser shall consult with each other on the timing, method, form and content of notifications to customers and suppliers of the transactions contemplated by this Agreement, and shall consider in good faith any comments or proposed changes received from the other.

7.3 Use of Seller Names. Seller hereby grants Purchaser the non-exclusive right and license to use the Seller Names solely to the extent necessary to allow Purchaser to market, distribute and sell the Products, utilizing the labels and packaging and coupons included in the Purchased Assets bearing such Seller Names. Such right and license shall extend after the Closing Date until such a date when the Inventory is exhausted.

7.4 Further Assurances. Following the Closing and, for no further consideration, each of the Parties shall, and shall cause its Affiliates to, execute, acknowledge and deliver such assignments, transfers, consents, assumptions and other documents and instruments and take such other commercially reasonable actions as may reasonably be requested to assign, convey or transfer to or vest in Purchaser and its designated Affiliates the Purchased Assets and the Assumed Liabilities contemplated by this Agreement to be transferred or assumed.

7.5 Assistance in Collecting Certain Amounts. From and after the Closing Date, Purchaser shall remit promptly to Seller any payments or other sums received by Purchaser that relate to any sales, shipments or other matters occurring before the Closing Date or that otherwise are properly for Seller’s account.

7.6 Bulk Transfer Laws. Purchaser acknowledges that Seller and its Affiliates have not taken, and do not intend to take, any action required to comply with any applicable bulk sale or bulk transfer Laws or similar Laws and hereby waives compliance therewith. Seller acknowledges that Purchaser and its Affiliates have not taken, and do not intend to take, any action required to comply with any applicable bulk sale or bulk transfer Laws or similar Laws and hereby waives compliance therewith.

7.7 Licenses and Additional Rights. To the extent that Seller has any right, asset or other property, whether tangible or intangible, but excluding any contract, license, agreement or commitment, that is necessary with respect to the Products and the Purchased Assets following the Closing in a manner consistent with Seller’s conduct with respect to the Products and the

Purchased Assets as of the date hereof, and would be a Purchased Asset hereunder but for the fact such right, asset or other property is not used primarily with respect to the Products by Seller prior to the Closing, Seller shall use commercially reasonable efforts to enter into an arrangement under which Purchaser is provided the benefits of such right, asset or other property and assumes any related obligations, provided, however that Seller shall have no obligation to make any payments to third parties in performing its obligations under this Section 7.7.

7.8 Employee Benefits.

(a) Within ninety (90) days of the Closing Date, Purchaser shall offer to employ each of the Personnel. Each such offer of employment shall be on terms and conditions, including employee benefit plans, that, taken as a whole, are comparable to the terms and conditions of employment, including employee benefit plans, provided to employees of Purchaser as of the date hereof. Each of the Personnel who accepts an offer of employment from Purchaser effective as of the Closing shall be referred to herein as a “Transferred Employee.”

(b) From and after the Closing Date, Purchaser shall recognize, or cause to be recognized, (i) any service credit accrued as of the Closing Date (including for purposes of determining eligibility and vesting) and (ii) any credit accrued as of the Closing Date towards satisfying deductible expense requirements and out-of-pocket expense limits, of all Transferred Employees and their respective dependents, for all purposes under Purchaser’s benefits and compensation arrangements other than benefit accruals. Purchaser and Seller agree that where applicable with respect to any medical or dental benefit plan of Purchaser, Purchaser shall waive, with respect to each Transferred Employee, any pre-existing condition exclusion (to the extent such exclusion would not have applied to such Transferred Employee under Seller’s medical or dental benefit plan).

(c) Purchaser shall provide continuation health care coverage to all Transferred Employees and their qualified beneficiaries who experience a “qualifying event” after the Closing Date in accordance with and to the extent required under the continuation health care coverage requirements of COBRA. Seller shall be responsible for providing continuation coverage and all related notices to the extent required by Law to any Transferred Employees (or qualified beneficiary) who experience a “qualifying event” under COBRA on or before the Closing Date.

Article VIII.

Indemnification

8.1 Indemnification by Seller. Subject to the provisions of this Article VIII, Seller will defend, indemnify and hold harmless Purchaser, its successors and assigns (each a “Purchaser Indemnified Party”), from and against any and all penalties, assessments, fines, fees, suits, actions, causes of action, judgments, Taxes, awards and Liabilities, including reasonable attorneys’ fees (collectively, “Losses”) arising from or relating to the following:

(a)

any Retained Liability as defined in section 2.4 of this Agreement;

(b)

any breach by Seller of any of its covenants or agreements contained in this Agreement; and

(c)

any breach of any representation or warranty of Seller contained in this Agreement.

8.2 Indemnification by Purchaser. Subject to the provisions of this Article VIII, Purchaser agrees to defend, indemnify and hold harmless Seller, its successors and assigns (each a “Seller Indemnified Party”), from and against any and all Losses arising from or relating to the following:

(a)

any Assumed Liability as defined in section 2.3 of this Agreement;

(b)

any breach by Purchaser of any of its covenants or agreements contained in this Agreement; or

(c)

any breach of any representation or warranty of Purchaser contained in this Agreement.

8.3 Notice of Claims. If any of the Persons to be indemnified under this Article VIII (the “Indemnified Party”) has suffered or incurred any Loss, the Indemnified Party shall so notify the Party from whom indemnification is sought (the “Indemnifying Party”) promptly in writing, describing such Loss, the amount or estimated amount thereof, if known or reasonably capable of estimation, and the method of computation of such Loss, all with reasonable particularity and containing a reference to the provisions of this Agreement or any other agreement, instrument or certificate delivered pursuant hereto in respect of which such Loss shall have occurred. If any claim, action, suit or proceeding (in equity or at law) is instituted by a third party with respect to which the Indemnified Party intends to claim any Loss under this Article VIII (a “Third-Party Claim”), the Indemnified Party shall promptly notify the Indemnifying Party of such claim, action, suit or proceeding and offer to tender to the Indemnifying Party the defense of such claim, action, suit or proceeding. A failure by the Indemnified Party to give notice and to offer to tender the defense of any claim, action, suit or proceeding in a timely manner pursuant to this Section 8.3 shall not limit the obligation of the Indemnifying Party under this Article VIII, except to the extent such Indemnifying Party is actually prejudiced thereby.

8.4 Third-Party Claims.

(a) If an Indemnified Party gives notice pursuant to Section 8.3 of the assertion of a Third-Party Claim, the Indemnifying Party shall be entitled to participate in the defense of such Third-Party Claim and, to the extent that it wishes (unless the Indemnifying Party is also a Person against whom the Third-Party Claim is made and the Indemnified Party determines in good faith upon advice of outside counsel that joint representation would be inappropriate), to assume the defense of such Third-Party Claim with counsel of its choice. After notice from the Indemnifying Party to the Indemnified Party of its election to assume the defense of such Third-Party Claim, the Indemnifying Party shall not, so long as it diligently conducts such defense, be liable to the Indemnified Party under this Article VIII for any fees of other counsel or any other expenses with respect to the defense of such Third-Party Claim, in each case subsequently incurred by the Indemnified Party in connection with the defense of such Third-Party Claim, other than reasonable costs of investigation. If the Indemnifying Party assumes the defense of a Third-Party Claim, (w) such assumption will conclusively establish for purposes of this Agreement that the claims made in that Third-Party Claim are within the scope of and subject to indemnification, (x) no compromise or settlement of such Third-Party Claim may be effected by the Indemnified Party without the Indemnifying Party’s consent, (y) no compromise or settlement of such Third-Party Claim may be effected by the Indemnifying Party

without the Indemnified Party’s consent unless (A) there is no finding or admission that the Indemnified Party violated any Law or any rights of any Person and (B) the sole relief provided is monetary damages that are paid in full by the Indemnifying Party; and (z) the Indemnified Party shall have no liability with respect to any compromise or settlement of such Third-Party Claims effected without its consent. If notice is given to an Indemnifying Party of the assertion of any Third-Party Claim and the Indemnifying Party does not, within twenty (20) days after the Indemnified Party’s notice is given, give notice to the Indemnified Party of its election to assume the defense of such Third-Party Claim, the Indemnifying Party will be bound by any determination made in such Third-Party Claim or any compromise or settlement effected by the Indemnified Party.

(b) The Indemnifying Party shall permit the Indemnified Party to participate in, but not control, the defense of any such Third-Party Claim through counsel chosen by the Indemnified Party; provided, that the fees and expenses of such counsel shall be borne by the Indemnified Party.

(c) With respect to any Third-Party Claim subject to indemnification under this Article VIII, (i) each of the Indemnified Party and the Indemnifying Party, as the case may be, shall keep the other fully informed in all material respects of the status of such Third-Party Claim and any related proceedings at all stages thereof where such Person is not represented by its own counsel, and (ii) the parties agree to render to each other such assistance as they may reasonably require of each other and to cooperate in good faith with each other to defend any Third-Party Claim.

8.5 Survival. The representations and warranties contained herein shall survive for eighteen (18) months following the Closing Date. Any claims asserted in good faith with reasonable specificity (to the extent known at such time) and in writing by notice from the Indemnified Party to the Indemnifying Party on or prior to the first anniversary of the Closing Date shall survive until finally resolved.

8.6 Limitations on Indemnification of Purchaser Indemnified Parties.

(a) An Indemnified Party shall not be entitled to indemnification under Section 8.1(c), (i) for any individual item or series of related items where the Loss relating thereto is less than [***] (the “De Minimis Limitation”) and (ii) in respect of each individual item or series of related items where the Loss relating thereto is equal to or greater than the De Minimis Limitation, unless the aggregate amount of all such Losses exceeds an amount equal to [***] (the “Deductible”), in which event Seller shall be required to pay only the amount of such Losses that exceed the Deductible.

(b) The Purchaser Indemnified Parties shall have no right to recover any amounts under Section 8.1(c) in excess of [***] (the “Cap”).

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

8.7 Losses Net of Insurance. The amount of any Loss for which indemnification is provided under Section 8.1 or Section 8.2 shall be net of (i) any amounts actually recovered by the Indemnified Party pursuant to any indemnification by or indemnification agreement with any third party, any tax benefits actually realized relating to the Purchased Assets (including the utilization of a Tax loss or Tax credit carried forward) by the Indemnified Party and (ii) any insurance proceeds actually received as an offset against such Loss, in each case, after deducting any related costs and expenses, including the aggregate cost of pursuing any related insurance claims and any related increases in insurance premiums or other chargebacks.

8.8 Right of Setoff. Upon notice specifying in reasonable detail the basis therefor, either Purchaser or Seller may set off any amounts due or payable pursuant to this Article VIII against amounts otherwise due or payable under this Agreement. The exercise of such right of setoff by Purchaser or Seller in good faith, whether or not ultimately determined to be justified, will not constitute an event of default hereunder.

8.9 Sole Remedy. Subject to Section 10.11, each Party acknowledges and agrees that the remedies provided for in this Article VIII shall be its sole and exclusive remedy with respect to the subject matter of this Agreement. Notwithstanding anything to the contrary contained in the foregoing, nothing herein shall (a) limit the liability of any Party for knowing and intentional fraud or willful misconduct or (b) prevent or restrict any Person who is a party to any Ancillary Agreement from obtaining monetary damages or any other legal or equitable relief in connection with the breach of such agreement.

8.10 Indemnity Payments. In the event that any Party agrees to or is determined to have an obligation to reimburse the other Party for Losses as provided in this Article VIII, the Indemnifying Party shall promptly pay such amount to the Indemnified Party in U.S. dollars via wire transfer of immediately available funds to the accounts specified in writing by the Indemnified Party. All payments made pursuant to this Article VIII shall be treated for Tax purposes as an adjustment to the Purchase Price, unless otherwise required by applicable Law.

8.11 No Consequential Damages. NOTWITHSTANDING ANYTHING TO THE CONTRARY CONTAINED HEREIN, NO PARTY TO THIS AGREEMENT OR ANY ANCILLARY AGREEMENT SHALL BE LIABLE TO OR OTHERWISE RESPONSIBLE TO THE OTHER PARTY OR ANY AFFILIATE OF THE OTHER PARTY FOR LOST REVENUES OR PROFITS OR INCIDENTAL, CONSEQUENTIAL, PUNITIVE OR EXEMPLARY DAMAGES THAT ARISE OUT OF OR RELATE TO THIS AGREEMENT OR ANY ANCILLARY AGREEMENT OR THE PERFORMANCE OR BREACH HEREOF OR THEREOF OR ANY LIABILITY RETAINED OR ASSUMED HEREUNDER OR THEREUNDER, EXCEPT TO THE EXTENT THAT SUCH DAMAGES WERE ACTUALLY PAID TO A THIRD PARTY PURSUANT TO A THIRD PARTY CLAIM.

Article IX.

Product Returns, Rebates and Chargebacks

9.1 NDC Numbers. Purchaser shall use commercially reasonable efforts to establish its own National Drug Code (“NDC”) numbers with respect to the Products as soon as practicable after the Closing. Purchaser shall begin to use the new NDC numbers for the Products as soon as practicable after receiving them.

9.2 Product Returns.

(a) Purchaser shall, or shall cause all of its distributors to, process and be financially responsible for all returns of Products made after the Closing Date. To be clear, Purchaser shall not be responsible for any Product Liability related to or arising out of the distribution of Product prior to the Closing Date.

(b) For any Product that is returned to Seller, Seller will promptly seek Buyer’s instructions for disposition, at Buyer’s expense, of such returned Product, and if such instructions are not received within thirty (30) days, Seller will destroy, or cause to be destroyed, all such Product and will provide Purchaser a report of such Product returned, including documentation sufficient to determine any appropriate customer reimbursement or credit and Seller’s invoice and reasonable documentation regarding any out-of-pockets costs for such destruction. Any reimbursement or credit shall be processed according to Purchaser’s then-current returned goods policy. Purchaser shall reimburse Seller for any out-of-pockets costs for destruction of returned Product within thirty (30) days of receipt of Seller’s invoice therefor.

9.3 Government Rebates. Responsibility for rebates pursuant to any government rebate programs with respect to government claims for Products (“Government Rebates”) shall be allocated between Seller and Purchaser as follows:

(a) Seller shall be responsible for all Government Rebates with respect to Products dispensed to patients on or prior to the Closing Date.

(b) Purchaser shall be responsible for all Government Rebates with respect to Products dispensed to patients beginning on the day following the Closing Date.

(c) Purchaser shall have the right to request through Seller any claims level data (dispense date) contained in any report from a state rebate program which shall be used for purposes of determining the date of such claim or for state rebate dispute purposes. In the event Purchaser determines an invoice or claim for a Government Rebate should be disputed, Seller shall cooperate with Purchaser to dispute such claim or invoice.

(d) To the extent that information related to Government Rebates is received with respect to the calendar quarter that includes the Closing Date, and such information does not include a dispense date, (i) Seller shall be responsible for the amount of such Government Rebates which shall be equal to the product of (x) a fraction, the numerator of which is the number of days in the period beginning the first day of such calendar quarter and ending on the Closing Date, and the denominator of which is the number of days in such calendar quarter, and (y) the amount of the Government Rebate and (ii) Purchaser shall be responsible for the amount of such Government Rebates which shall be equal to the product of (x) one (1) minus the fraction determined pursuant to clause (i)(x) above and (y) the amount of the Government Rebate.

9.4 Commercial Rebates. Responsibility for commercial rebates with respect to Products (“Commercial Rebates”) shall be allocated between Seller and Purchaser as follows:

(a) Seller shall be responsible for all Commercial Rebates with respect to Products dispensed to patients on or prior to the Closing Date.

(b) Purchaser shall be responsible for all Commercial Rebates with respect to Products dispensed to patients beginning on the date following the Closing Date.

(c) To the extent that information related to Commercial Rebates is received with respect to the calendar quarter that includes the Closing Date, and such information does not include a dispense date, (i) Seller shall be responsible for the amount of such Commercial Rebates which shall be equal to the product of (x) a fraction, the numerator of which is the number of days in the period beginning the first day of such calendar quarter and ending on the Closing Date, and the denominator of which is the number of days in such calendar quarter, and (y) the amount of the Commercial Rebate and (ii) Purchaser shall be responsible for the amount of such Commercial Rebates which shall be equal to the product of (x) one (1) minus the fraction determined pursuant to clause (i)(x) above and (y) the amount of the Commercial Rebate.

9.5 Chargeback Claims. Seller shall be financially and legally responsible for all chargeback claims (“Chargeback Claims”) related to Products sold by each wholesale and account-level customer (including hospitals, health systems and integrated delivery networks), as evidenced in the invoice date within the Chargeback Claims, prior to the Closing Date. Purchaser shall process and be financially and legally responsible for all Chargeback Claims related to Products sold by each wholesale and account-level customer (including hospitals, health systems and integrated delivery networks) on or after the Closing Date. The date on which Products shall be deemed to have been sold pursuant to the preceding sentence shall be the date on which it was shipped by the applicable wholesaler. Notwithstanding the foregoing, the Parties acknowledge that the VA National Acquisition Center must approve the removal of Products from Seller’s Federal Supply Schedule before the responsibility of processing such claims is transferred from Seller to Purchaser. Until such approval is obtained, Seller shall continue to be responsible for processing the Federal Supply Schedule Chargeback Claims on Purchaser’s behalf, and Purchaser shall reimburse Seller for same. Purchaser and Seller agree that (A) Seller’s financial liability for the Chargeback Claims shall be limited to those commercial customers with which Seller has chargeback obligations as of the Closing Date, and (B) any such chargebacks issued by Seller shall be made in accordance with terms and conditions of Seller’s obligations as of the Closing Date with respect to each customer and shall be solely based on the terms and conditions of Seller’s agreements with the respective customer, as such terms and conditions existed as of the Closing Date. Seller shall utilize records from third party rebate administrators to demonstrate which chargebacks relate to Products sold by a wholesaler or distributor, as evidenced in the invoice date within the Chargeback Claims, prior to the Closing Date for purposes of determining Seller’s obligation.

9.6 Misdirected Claims.

(a) If Purchaser or Seller (the “Non-Responsible Party”) receives an invoice with respect to a Government Rebate, a Commercial Rebate or a Chargeback Claim that is the responsibility of the other Party (the “Responsible Party”), such Non-Responsible Party shall promptly provide a copy of such invoice to the Responsible Party and such Responsible Party shall have fifteen (15) days following receipt of such invoice to notify the Non-Responsible Party

that it intends to dispute such invoice. If the Responsible Party does not so notify the Non-Responsible Party within such fifteen (15) day period, such Non-Responsible Party shall be permitted to remit payment in respect of such invoice on the Responsible Party’s behalf and the Responsible Party shall reimburse the Non-Responsible Party for such payment. If the Responsible Party provides such notice to the Non-Responsible Party within such fifteen (15) day period then the Responsible Party shall promptly initiate a dispute of such invoice at its sole cost and expense and shall be liable for all reasonable costs and expenses (including reasonable attorney fees) of the Non-Responsible Party required to prosecute the disputed invoice. In the event that an invoice is disputed under this Section by the Responsible Party, the Non-Responsible Party shall not remit payment in respect of such invoice without the Responsible Party’s prior written consent; provided, however, that any late fees, interest or other penalties that are ultimately owing due to delayed payment on such invoice shall be satisfied by the Responsible Party; and provided further that notwithstanding the foregoing, the Non-Responsible Party may, in its sole discretion, pay any such disputed invoice without the consent of the Responsible Party, but in such case the Non-Responsible Party shall be entitled to reimbursement by the Responsible Party only with respect to amounts if any, that are finally owing following settlement of the related dispute.

(b) To the extent that a Non-Responsible Party remits a payment payable by the Responsible Party, the Responsible Party shall reimburse the Non-Responsible Party on or before the date that is thirty (30) days following receipt of such invoices from such Non-Responsible Party; provided, however, that such invoices describe in reasonable detail the payments made by such Non-Responsible Party.

9.7 Reporting.

(a) Each Party shall use its commercially reasonable efforts to (A) file all necessary documentation with Governmental Authorities required as a result of the transactions contemplated by this Agreement (including any necessary documentation with Medicaid, Medicare Part D, PHS 340B, TriCare and VA/DOD) and (B) reasonably assist the other Party in implementing the allocation of liability and financial and legal responsibility set forth in this Section 7.13.

(b) With respect to the reporting of Average Manufacturer Price (as defined in the Social Security Act, 42 U.S.C. §1396r-8(k)) and Best Price (as defined in the Social Xxxxxxxx Xxx, 00 X.X.X. § 0000x-0(x)(0)(X)), or other data or information regarding sales, timing and pricing, for the Products as required by the applicable Governmental Authority, each Party will in a timely manner provide to the other Party any information required to comply with its reporting requirements as determined by the other Party in its reasonable discretion. Each Party warrants that all information provided to the other Party pursuant to this Section will be complete and accurate in all material respects and that the other Party may rely upon such information in fulfilling its regulatory reporting obligations. The Parties agree to cooperate with each other to correct in a timely manner any inaccuracies and deficiencies in such information identified by either Party. Each Party shall treat the information provided to such Party from the other Party under this Section as confidential information of the other Party and agrees that such disclosure is solely for the purpose of enabling such Party to comply with its regulatory reporting obligations. Each Party agrees to use commercially reasonable efforts to limit access to such information by its employees and advisers to those who are responsible for reporting such information or otherwise have a need to know in connection with such purpose and expressly shall use its reasonable efforts to not allow access to such information to any personnel responsible for the marketing or the setting of prices for the applicable Products.

Article X.

Miscellaneous

10.1 Notices. Notices or other communications required or permitted hereunder shall be deemed to have been sufficiently given (a) four (4) Business Days following deposit in the mails if sent by registered or certified mail, postage prepaid; (b) when sent, if sent by facsimile transmission; (c) when delivered, if delivered personally to the intended recipient; and (d) one (1) Business Day following deposit with an overnight courier service, in each case addressed as follows:

to Seller:

Cornerstone Therapeutics, Inc

0000 Xxxxxxxx Xxxxx Xxxxx

Xxxx, XX 00000

Attention: General Counsel

with a copy (which shall not constitute notice) to:

Smith, Anderson, Blount, Dorsett, Xxxxxxxx & Xxxxxxxx, L.L.P.

Xxxxx Fargo Capitol Center

000 Xxxxxxxxxxxx Xxxxxx, Xxxxx 0000

Xxxxxxx, Xxxxx Xxxxxxxx 00000

Attention: Xxxxx X. Xxxxxxx

to Purchaser:

Vansen Pharma, Inc.

0000-0000 xxxx. Xx Xxxxxxxxxxx X.,

Xxxxxxxxx, Xxxxxx,

XXXXXX, X0X 0X0

Attention: Xxxxxxx Xxxxxxxx, President

10.2 Amendment; Waiver. Any provision of this Agreement may be amended or waived if, and only if, such amendment or waiver is in writing and signed (a) in the case of an amendment, by Purchaser and Seller and (b) in the case of a waiver, by the Party against whom the waiver is to be effective. No failure or delay by any Party in exercising any right, power or privilege hereunder shall operate as a waiver thereof, nor shall any single or partial exercise thereof preclude any other or further exercise thereof or the exercise of any other right, power or privilege.

10.3 Assignment. No Party to this Agreement may assign any of its rights or obligations under this Agreement without the prior written consent of the other Parties, except that each Party may, without any other Party’s consent, assign its rights or obligations to an Affiliate; provided, however, that no such assignment by any Party shall relieve such Party of any of its obligations hereunder.

10.4 Entire Agreement. This Agreement, together with the Ancillary Agreements, contains the entire agreement among the Parties with respect to the subject matters hereof and thereof and supersedes all prior agreements and understandings, oral or written, with respect to such matters, except for the Confidential Disclosure Agreement, which shall remain in full force and effect for the term provided for therein.

10.5 Parties in Interest. This Agreement shall inure to the benefit of and be binding upon the Parties and their respective successors and permitted assigns.

10.6 Public Disclosure. Any press releases announcing the execution of this Agreement or the consummation of the transactions contemplated hereby shall be issued in such form as mutually agreed upon by Seller and Purchaser. Except as may be required to comply with the requirements of any applicable Laws or the rules and regulations of each stock exchange upon which the securities of Purchaser or Seller are listed, if any (in which case such Party shall promptly notify the other Parties and provide the other Parties with a copy of the contemplated disclosure prior to submission or release, as the case may be, unless notifying is impracticable due to circumstances beyond such Party’s control), no other press release or similar public announcement or communication shall, at any time, be made by Purchaser or Seller or caused to be made by them concerning this Agreement or the transactions contemplated hereby unless the disclosing Party shall have consulted with the other Parties in advance with respect thereto and such other Parties consent in writing to such release, announcement or communication. Notwithstanding anything to the contrary in the foregoing, each Party shall be permitted to make such releases or public announcements or communications to the extent consistent with previous disclosures made in accordance with Section 10.6.

10.7 Expenses. Except as otherwise provided in this Agreement, whether or not the Closing takes place, all costs and expenses incurred in connection with this Agreement and the transactions contemplated hereby shall be paid by the Party incurring such costs and expenses.

10.8 Governing Law; Jurisdiction; No Jury Trial.

(a) The interpretation and construction of this Agreement, and all matters relating hereto, shall be governed by the Laws of the State of New York, without regard to the choice of Law principles thereof.

(b) Each Party consents to the exclusive jurisdiction of the Federal and State courts located in New York City, New York for any action to compel arbitration, in aid of arbitration or to maintain the status quo or prevent irreparable harm prior to the appointment of the Arbitrator, and to the non-exclusive jurisdiction of such courts for enforcement of any arbitral award rendered in accordance with Section 10.10 herein. Each of the Parties (i) consents to the jurisdiction of each such court in any such suit, action or proceeding, (ii) waives any objection that it may have to the laying of venue in any such suit, action or proceeding in any such court and (iii) agrees that service of any court paper may be made in such manner as may be provided under applicable Laws or court rules governing service of process as well as in the manner provided for the giving of notices in Section 10.1.

10.9 Arbitration; Mediation.

(a) Any dispute, controversy or claim involving any Party or its Affiliates arising out of or relating to this Agreement or any Ancillary Agreements (a “Dispute”), shall first be submitted to a senior business person of each of Purchaser and Seller, each with authority to resolve the Dispute. If such Persons cannot resolve the Dispute within thirty (30) days after notice of a Dispute, either Party may submit such Dispute to nonbinding mediation in accordance with the Commercial Mediation Procedures of the American Arbitration Association (“AAA”). Such mediation shall be attended on behalf of each Party by a senior business person with authority to resolve the Dispute. Any period of limitations that would otherwise expire between the initiation of a mediation and its conclusion shall be extended until twenty (20) days after the conclusion of the mediation. The costs of mediation shall be shared equally by the parties to the mediation.

(b) Any Dispute that cannot be resolved for any reason by mediation within sixty (60) days of notice by one Party to the other of the existence of a Dispute (unless the Parties agree in writing to extend that period) shall be finally resolved by arbitration in accordance with the Commercial Arbitration Rules of the AAA (“AAA Rules”) and the Federal Arbitration Act, 9 U.S.C. §1 et seq. The arbitration shall be conducted in New York City, New York. There shall be a panel of three (3) arbitrators (hereinafter “the Panel”) appointed in accordance with the following. Each party will select one independent, impartial and conflicts-free neutral, and those two neutrals will select a third independent, impartial and conflicts-free neutral. None of the neutrals selected for the Panel may be current or former employees, officers, or directors of each party, its subsidiaries or Affiliates. The arbitration shall be conducted over the course of consecutive business days and weeks.

(c) The Panel shall decide the Dispute in accordance with the substantive law of New York. THE PANEL SHALL NOT AWARD EITHER PARTY NON-COMPENSATORY, INCIDENTAL, CONSEQUENTIAL, PUNITIVE OR EXEMPLARY DAMAGES, EXCEPT AS MAY BE REQUIRED BY APPLICABLE LAW, UNLESS SUCH PARTY IS SEEKING SUCH TYPE OF DAMAGES ON THE BASIS THAT IT WAS REQUIRED TO PAY SUCH TYPE OF DAMAGES TO A THIRD PARTY. The award of the Panel may be entered in any court of competent jurisdiction.

(d) The costs of the arbitration including the fees and expenses of the Panel and reasonable attorneys’ fees and expenses shall be borne by the non-prevailing Party and awarded by the Panel in the award. In determining the reasonableness of the attorneys fees the Panel shall take into account all relevant facts and circumstances, including but not limited to the amount of damages sought and the amount of the award.

10.10 Remedies. Except as otherwise provided herein, any and all remedies herein expressly conferred upon a Party will be deemed cumulative with and not exclusive of any other remedy conferred hereby, or by law or equity, upon such Party.

10.11 Counterparts. This Agreement may be executed in two or more counterparts, each of which shall be deemed an original, and which together shall constitute one and the same agreement and shall become effective when one or more counterparts have been signed by each of the Parties and delivered to the other Party, it being understood that both Parties

need not sign the same counterpart. The exchange of copies of this Agreement or amendments thereto and of signature pages by facsimile transmission or by email transmission in portable document format, or similar format, shall constitute effective execution and delivery of such instrument(s) as to the Parties and may be used in lieu of the original Agreement or amendment for all purposes. Signatures of the Parties transmitted by facsimile or by email transmission in portable document format, or similar format, shall be deemed to be original signatures for all purposes.

10.12 Headings. The heading and section references herein and the table of contents hereto are for convenience purposes only, do not constitute a part of this Agreement and shall not be deemed to limit or affect any of the provisions hereof.

10.13 Severability. The provisions of this Agreement shall be deemed severable and the invalidity or unenforceability of any provision shall not affect the validity or enforceability of the other provisions hereof. If any term or other provision of this Agreement, or the application thereof to any Person or any circumstance, is invalid, illegal or unenforceable, (a) a suitable and equitable provision shall be substituted therefor in order to carry out, so far as may be valid and enforceable, the intent and purpose of such invalid or unenforceable provision and (b) the remainder of this Agreement and the application of such provision to other Persons or circumstances shall not be affected by such invalidity, illegality or unenforceability, nor shall such invalidity, illegality or unenforceability affect the validity or enforceability of such provision, or the application thereof, in any other jurisdiction.

10.14 Currency. All monies set forth in this Agreement are to be properly paid in United States currency.

10.15 Guaranty. The Purchaser agrees that if at any time it transfers all or any substantial part of its assets to a related or successor company, it will so notify Seller, and, if Seller so reasonably requests, arrange, on behalf of itself, its Affiliates, and its Affiliates’ successors and assigns, for such related or successor company to guarantee to Seller the performance by Purchaser of all of Purchaser’s duties and obligations under this Agreement, including repurchase of returned Products and other payment obligations, defense and indemnity obligations, and payment of all damages, liability, costs, expenses and other amounts that may be payable by Seller, or recoverable by Purchaser from Seller by virtue of this Agreement, and to agree to immediately perform any duties and obligations under this Agreement in the event Purchaser fails to do so when due upon written demand by Seller.

IN WITNESS WHEREOF, Purchaser and Seller have caused this Agreement to be signed by their respective officers thereunto duly authorized as of the date first written above.


Purchaser:

By	/s/ Xxxxxxx Xxxxxxxx
	Name:	Xxxxxxx Xxxxxxxx
	Title:	President


Seller:

By	/s/ Xxxxxx Xxxxxx
	Name:	Xxxxxx Xxxxxx
	Title:	EVP

EXHIBIT AND SCHEDULE INDEX


Exhibits:
Exhibit A		Products
Exhibit B		Assignment and Assumption Agreement
Exhibit C		Xxxx of Sale
Exhibit D		Transition Services Agreement
Exhibit E		Assignment and Assumption Agreement
Exhibit F		Copromotion Agreement

Schedules:
Schedule 2.1(a)*		Assumed Contracts
Schedule 2.6*		Inventory Valuation
Schedule 2.10*		Provisional Coupon Prefund Balance
Schedule 5.3*		Non-contravention
Schedule 5.5*		Financial Information
Schedule 5.15*		Regulatory Matters
Schedule 5.15(f)*		Regulatory Fees
Schedule 5.17*		Personnel

*	Not filed herewith pursuant to Item 601(b)(2) of Regulation S-K. The registrant will supplementally provide a copy of this schedule or exhibit to the Securities and Exchange Commission upon request.

EXHIBITS TO VANSEN APA


Exhibit A		Products

EXHIBIT A

PRODUCTS

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 200mg 20 Tablets in 1 Blister Pack

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 400mg 2 Tablets in 1 Blister Pack

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 400mg 20 Tablets in 1 Blister Pack

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 400mg 28 Tablets in 1 Blister Pack

00000-0000-00 cefditoren pivoxil film coated Tablets 200mg 20 Tablets in 1 Blister Pack

00000-0000-00 cefditoren pivoxil film coated Tablets 400mg 20 Tablets in 1 Blister Pack

EXHIBITS TO VANSEN APA


Exhibit B		Assignment and Assumption Agreement — Assumed Contracts

ASSIGNMENT AND ASSUMPTION AGREEMENT

ASSIGNMENT AND ASSUMPTION AGREEMENT, entered into on March 7, 2012 by Cornerstone Therapeutics Inc., a Delaware corporation (the “Seller”) and Vansen Parma, a Canadian corporation (the “Purchaser”).

WITNESSETH

WHEREAS, the Purchaser and the Seller are parties to that certain Asset Purchase Agreement dated March 7, 2012 by and between Purchaser and Seller (the “Agreement”).

WHEREAS, pursuant to the Agreement, the Seller agreed to assign and the Purchaser agreed to assume certain contracts of the Seller, including those listed on Schedule 2.1(a) attached to this Assignment and Assumption (the “Transferred Contracts”).

NOW, THEREFORE, in consideration of the foregoing premises and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Purchaser and the Seller hereby agree as follows:

1. Effective from and after the Closing, the Seller hereby assigns to the Purchaser, free and clear of all Liens, the Transferred Contract.

2. Effective from and after the Closing, the Purchaser hereby assumes the Transferred Contract.

3. This Assignment and Assumption Agreement shall be construed and enforced in accordance with applicable federal law and the laws (other than the conflict of law rules) of the State of New York.

4. In the event that any provision of this Assignment and Assumption Agreement is construed to conflict with a provision of the Agreement, the provision in the Agreement shall be deemed controlling.

5. This Assignment and Assumption Agreement shall bind and shall inure to the benefit of the respective parties and their assigns, transferees and successors.

[The rest of this page intentionally left blank]

IN WITNESS WHEREOF, the undersigned have executed this Assignment and Assumption Agreement as of the date first above written.


CORNERSTONE THERAPEUTICS INC. (as successor to Cornerstone Biopharma, Inc. and parent of Aristos Pharmaceuticals, as applicable)

By
		Name:
		Title:


PURCHASER

By
		Name:
		Title:

EXHIBITS TO VANSEN APA


Exhibit C		Xxxx of Sale

XXXX OF SALE

XXXX OF SALE, made, executed and delivered on Xxxxx 0, 0000, Xxxxxxxxxxx by Therapeutics Inc., a Delaware corporation (the “Seller”), acting on behalf of itself and all of its subsidiary and affiliated companies, and Vansen Pharma, Inc., a Canadian corporation (the “Purchaser”).

WITNESSETH

WHEREAS, the Seller and the Purchaser are parties to that certain Asset Purchase Agreement dated March 7,2012 by and between Purchaser and Seller (the “Agreement”), providing for, among other things, the transfer and sale to the Purchaser of the Purchased Assets (such capitalized term and, except as defined herein, all other capitalized terms used herein shall have the same meanings ascribed to them in the Agreement), and on the terms and conditions provided in the Agreement.

WHEREAS, the Purchaser and the Seller now desire to carry out the intent and purpose of the Agreement by the Seller’s execution and delivery to the Purchaser of this instrument evidencing the sale, conveyance, assignment, transfer and delivery to the Purchaser of the Purchased Assets, subject to the Assumed Liabilities and subject to the terms and conditions of the Agreement.

NOW, THEREFORE, in consideration of the foregoing premises and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Seller does hereby, effective from and after the date hereof, sell, convey, assign, transfer and deliver unto the Purchaser and its successors and assigns, forever, the entire right, title and interest in, to and under the Purchased Assets, subject only to the Assumed Liabilities and subject to the terms and conditions of the Agreement and free and clear of Liens.

TO HAVE AND TO HOLD the Purchased Assets unto the Purchaser, its successors and assigns, FOREVER.

This Xxxx of Sale shall be construed and enforced in accordance with applicable federal law and the laws (other than the conflict of law rules) of the State of New York.

In the event that any provision of this Xxxx of Sale is construed to conflict with a provision of the Agreement, the provision of the Agreement shall be deemed to be controlling.

This instrument shall be binding upon and shall inure to the benefit of the respective successors and assigns of the Seller and the Purchaser.

[The rest of this page intentionally left blank]

IN WITNESS WHEREOF, this Xxxx of Sale has been duly executed and delivered by a duly authorized representative of the Seller on the date first above written.


CORNERSTONE THERAPEUTICS INC. (as successor to Cornerstone Biopharma, Inc. and parent of Aristos Pharmaceuticals, as applicable)

By
		Name:
		Title:

EXHIBITS TO VANSEN APA


Exhibit D		Transition Services Agreement

TRANSITION SERVICES AGREEMENT

This Transition Services Agreement (this “Agreement”), is effective as of March 7th, 2012 (the “Effective Date”), is made by and between Cornerstone Therapeutics Inc. (“Cornerstone”) and Vansen Pharma Inc (“Vansen”).

WITNESSETH:

WHEREAS, pursuant to the terms of an Asset Purchase Agreement dated March 7, 2012 between Cornerstone and Vansen (the “Asset Purchase Agreement”), Cornerstone has sold certain assets and granted certain licenses to Vansen in and for the Territory; and

WHEREAS, in connection with the Asset Purchase Agreement, Vansen desires and Cornerstone is willing, to provide certain warehousing, distribution and other transition services during the Operational Transition Period and during the Sales Force Transition Period (as hereinafter defined) with respect to Products (as hereinafter defined) on the terms and conditions set forth herein.

NOW, THEREFORE, in consideration of the agreements and covenants contained herein, the receipt and sufficiency of which are hereby acknowledged, the parties agree as follows:

1.	DEFINITIONS

1.1.	The following terms as used in this Agreement, whether used in the singular or the plural, shall have the meanings as set forth in this Article 1.

“Affiliate” shall mean any company or business entity directly or indirectly controlled by, controlling or under common control with a party to this Agreement. For this purpose, “control” shall mean the power, directly or indirectly, to direct or cause the direction of the management and policies of a company or business entity and control is conclusively presumed in case of direct or indirect ownership of more than 50% (fifty percent) of the voting stock of such company or the right to receive over fifty percent (50%) of the profits or earnings of an entity. Such other relationship as in fact results in actual control over the management, business and affairs of an entity shall also be deemed to constitute control.

“Business Day” means a day on which banks are open for business in the City of Montreal, but does not include a Saturday, Sunday or holiday in the State of North Carolina

“Customer Notice” shall have the meaning given such term in Section 2.8 hereof.

“Effective Date” shall have the meaning given such term in the introductory paragraph to this Agreement.

“Formulary Notice” shall have the meaning given such term in Section 2.9 hereof.

“FDA” means the US Food and Drug Administration

“Operational Transition Services” shall have the meaning given to such term in Section 2.1.

“Operational Transition Period” means the period from the Effective Date until April 1st 2012;

“Products” means:

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 200mg 20 Tablets in 1 Dose Pack

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 400mg 2 Tablets in 1 Blister Pack

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 400mg 20 Tablets in 1 Dose Pack

00000-0000-00 Spectracef® (cefditoren pivoxil) film coated Tablets 400mg 28 Tablets in 1 Dose Pack

00000-0000-00 cefditoren pivoxil film coated Tablets 200mg 20 Tablets in 1 Dose Pack

00000-0000-00 cefditoren pivoxil film coated Tablets 400mg 20 Tablets in 1 Dose Pack

“Recall” with respect to any Product, shall mean a “recall”, or “product withdrawal” or “stock recovery”, as those terms are defined in the Recall Procedures, and shall include any post-sale warning or mailing of information regarding such Product, including those warning or mailings described in the Recall Procedures.

“Recall Procedures” means the Product Recall Procedures reflected in Good Manufacturing Practices and Cornerstone’s SOP’sSOP’sStandard Operating Procedures.

“Regulatory Files” has the meaning ascribed thereto in the Asset Purchase Agreement.

“Statutory Provision” shall have the meaning given such term in Section 1.2(e) hereof.

“Sales Force Transition Period” means the period from the Effective Date until [***];

“Sales Force Transition Services” shall have the meaning given to such term in Section2.2 .

“Term” shall have the meaning given to such term in Article 6 hereof.

“Territory” means the country of US.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

1.2.	Interpretation

(1)

Unless the context otherwise requires in this Agreement, reference to:

(a)

one gender includes the others;

(b)

the singular includes the plural and the plural includes the singular;

(c)

a person includes a natural person, corporation, judicial entity, association, statutory body, partnership, limited liability company, joint venture, trust, estate, unincorporated organization or government, state or any political subdivision, instrumentality, agency or authority;

(d)

a party includes the party’s executors, administrators, successors and permitted assigns;

(e)

a statute, regulation or provision of a statute or regulation (“Statutory Provision”) includes:

(i)

that Statutory Provision as amended or re-enacted from time to time; and

(ii)

a statute, regulation or provision enacted in replacement of that Statutory Provision; and

(f)

money or ‘$’ is to dollars of United States.

(2)

Including and similar expressions are not words of limitation.

(3)

Where a word or expression is given a particular meaning, other parts of speech and grammatical forms of that word or expression have a corresponding meaning.

(4)

Headings and any table of contents or index are for convenience only and do not form part of this Agreement or affect its interpretation.

(5)

Any reference in this Agreement to “this Agreement” includes all schedules to this Agreement and all amendments, additions and variations thereto agreed between the parties. Any references to “articles”, “sections” and “schedules” in this Agreement shall be construed as references to the articles, sections and schedules of this Agreement.

(6)

A provision of this Agreement must not be construed to the disadvantage of a party merely because that party was responsible for the preparation of the Agreement or the inclusion of the provision in the Agreement.

(7)

If an act must be done on a specified day which is not a Business Day, it must be done instead on the next Business Day.

2.	TRANSITION SERVICES

2.1.

Operational Transition Services. Subject to the terms and conditions of this Agreement, during the Operational Transition Period, Vansen hereby retains

Cornerstone to provide, and Cornerstone hereby agrees to provide (or cause a third party contractor to provide) for Vansen, certain warehousing, distribution, customer service and accounts service, in connection with Vansen’s distribution of Products in the Territory including, without limitation, providing warehousing space, providing appropriate personnel to accept and warehouse inventory of Products shipped to its or its agents’ facilities, arranging for the shipping and delivery of Products to customers, providing certain administrative and support services in connection with Vansen distribution of Products in the Territory, providing certain regulatory, pharmacovigilance, medical information and quality assurance services consistent with Cornerstone past standards and maintaining the Regulatory Files for the Product in compliance with FDA standards and regulations, all as more specifically set forth in Schedule 2.1 attached hereto and made a part hereof (collectively, the “Operational Transition Services”). During the Operational Transition Period Cornerstone will ensure that appropriate personnel are available to provide the Transition Services. Vansen will reimburse Cornerstone for any out of pocket expenses incurred in providing the Operational Transition Services, within thirty days of receipt of an invoice reflecting such expenses.

2.2.	Sales Force Transition Services. Subject to the terms and conditions of this Agreement, during the Sales Force Transition Period, Vansen hereby retains Cornerstone to provide, and Cornerstone hereby agrees to provide (or cause a third party contractor to provide) for Vansen:

•

An employed sales force of [***], [***] and [***] that would report to a Vansen executive throughout the Sales Force Transition Period and

•

Administrative management of the sales force. This should include those Sales Force Transition Services listed on Schedule 2.2, including fleet, expense report management, PDMA compliance, payroll, benefits, SFA system management and administration of an incentive compensation plan (with incentive bonuses to be accrued but not paid) consistent with Cornerstone’s past practices.

At the end of [***], Cornerstone will invoice Vansen for the cost of all Sales Force Transition Services provided up to such date, including:

[***]

At the end of the Sales Force Transition Period, Cornerstone will invoice Vansen for the remaining cost of all Sales Force Transition Services rendered up to such time.

All invoices should be paid within 5 business days of receipt by wire transfer.

No fleet termination charges will be passed on to Vansen.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

2.3.	Termination of Services. Vansen may terminate any particular Sales Force Transition Service, in whole or in part, upon thirty (30) Business Days’ prior written notice to Cornerstone.

2.4.	Compliance with Laws. Each party shall, and shall cause its respective employees to, comply with all provincial, federal, local and foreign laws, regulations and orders which may be applicable to the Transition Services.

2.5.

Standard of Performance. Cornerstone shall ensure that the Transition Services are provided commensurate with the standard of care, and as applicable in accordance with good manufacturing practices, as used by CORNERSTONE in the performance of the same or similar functions for itself in relation to Products immediately preceding the Effective Date.

2.6.

Title and Risk of Loss. Title to the Products subject to Transition Services hereunder shall at all times remain with Vansen and, subject to Article 5, Vansen assumes all risk of loss of such Products as of the Effective Date. The Products while in Cornerstone’s possession and control will be insured by Vansen at Vansen’s expense. CORNERSTONE shall have no risk or liability for loss or casualty to the Products except in the event that any loss or damage to such goods is shown to have resulted from the gross negligence or willful misconduct by CORNERSTONE.

2.7.	Product Returns. The respective responsibilities of CORNERSTONE and Vansen for returns of the Products are set forth in the Asset Purchase Agreement

2.8.

Customers. CORNERSTONE shall deliver the notice to be sent to all contracted customers, buying groups, trade customers, and wholesalers, notifying them of the transfer of the sales, distribution and customer support services for the Product from CORNERSTONE to Vansen, which notice shall be in the form set forth in Schedule 2.6 (the “Customer Notice”) and shall be transmitted within five (5) Business Days of receipt of written notice from Vansen which in no event shall be later than five (5) Business Days following the end of the Effective Date.

2.9.

Formularies and Private Health Insurers. CORNERSTONE shall deliver the notice to be sent to public insurers, including formularies, and to private insurers, as applicable, notifying them of the transfer of the sales, distribution and customer support services for the Product from CORNERSTONE to Vansen, which notice shall be in the form set forth in Schedule 2.7 attached hereto (the “Formulary Notice”) and shall be transmitted on the same date as the Customer Notice.

2.10.

[intentionally omitted].

2.11.

Pricing of Product. If, during the term of this Agreement and subject to this Section 2.11, CORNERSTONE shall sell Products for Vansen’s account, such sales shall be at the [***]. Vansen shall not change the price or other terms and conditions of sale without Cornerstone’s prior written consent. Where applicable and until the Effective Date of a notice provided in accordance with this Section 2.11, any contract prices to specific customers (including without limitation applicable discounts, chargebacks and rebates) in effect immediately prior to the Effective Date shall continue in effect.

2.12.

Cornerstone Sales Prior to Effective Date. CORNERSTONE shall, for its own account, sell and distribute Products in the Territory for all purchase orders that CORNERSTONE received and which have been shipped to its wholesalers or other customers prior to the Effective Date. All costs and profits related to such sales shall be entirely for the benefit of CORNERSTONE and the income therefrom shall correspondingly accrue to CORNERSTONE and be recorded by CORNERSTONE.

2.13.

Sales during Sales Force Transition Period. During the Sales Force Transition Period, all sales and distribution of the Product in the Territory to wholesalers or other customers shall be for the ultimate benefit of Vansen. , Cornerstone will make no sales of Products during the Operational Transition Period or the Sales Force Transition Period.

2.14.

Vansen Sales. As of the Closing Date of the Asset Purchase Agreement, all sales and distribution of the Product in the Territory to wholesalers or other customers shall be the sole responsibility of Vansen and be recorded by Vansen.

2.15.

Audit. Upon reasonable prior written notice during the Transition Period and for 3 months thereafter, CORNERSTONE shall allow Vansen and its representatives to inspect CORNERSTONE’s books and records in Cornerstone’s offices relating to the Transition Services for the purposes of confirming CORNERSTONE’s compliance with this Agreement, provided that a CORNERSTONE representative is present during any such inspection. Vansen, or its representative(s), shall conduct such audit, at its expense, during normal business hours at a time on which the parties have mutually agreed to, and in such a manner that does not unreasonably interfere with CORNERSTONE’s normal business activities.

TAXES

Vansen Responsible for Taxes. Any and all taxes (excluding income taxes based solely upon CORNERSTONE’s net income) relating to Transition Services provided under this Agreement, including, without limitation, sales, use, goods and services and excise taxes required to be paid by any tax authority shall be borne by Vansen. Official receipts indicating proof of payment of any such taxes shall be secured and made available to CORNERSTONE upon request as evidence of payment.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

4.	[INTENTIONALLY BLANK]

5.	[INTENTIONALLY BLANK]

6.	TERM AND TERMINATION

6.1.

This Agreement shall be effective as of the Effective Date and shall continue in effect until the last day of the Sales Force Transition Period unless earlier terminated as provided in this Article 6 (the “Term”).

6.2.

This Agreement may be terminated by written notice given by either party as follows:

(1)

If the other party shall be in breach of any material obligation hereunder, and has not cured such breach within thirty (30) Business Days after receipt of a notice from the non-breaching party requesting the correction of such breach. Such termination shall be effective upon failure of the breaching party to cure such breach within the specified time period; or

(2)

If the other party shall be in breach of any material obligations under the Asset Purchase Agreement or any Related Agreement, and has not cured such breach within thirty (30) Business Days after receipt of a notice from the non-breaching party requesting the correction of such breach. Such termination shall be effective upon failure of the breaching party to cure such breach within the specified time period; or

(3)

Upon the filing or institution of any bankruptcy, reorganization, liquidation or receivership proceedings by the other party, or upon the failure by the other party for more than thirty (30) Business Days to discharge any such actions against it. Such termination shall be effective upon receipt of the notice; or

(4)

If the force majeure event specified in Section 7.1 shall continue for more than thirty (30) consecutive days.

6.3

This Agreement may be terminated by Vansen upon thirty (30) Business Days prior written notice to CORNERSTONE.

6.4

The termination of this Agreement shall not affect the rights and obligations of the parties arising prior to such termination. Termination under this Article 6 shall relieve and release all parties from any liabilities and obligations under this Agreement other than those specifically set forth in this Article 6, those that survive termination in accordance with Section 7.14 and any and all obligations to indemnify the other party in accordance with Article 5. Notwithstanding any provision of the Asset Purchase Agreement or any Related Agreement to the

contrary, termination of this Agreement shall not affect the rights and obligations of the parties under the Asset Purchase Agreement and the Related Agreements.

7.	MISCELLANEOUS

7.1.

Force Majeure. The parties shall not be liable for the failure or delay in performing any obligation under this Agreement, if and to the extent such failure or delay is due to (a) acts of God; (b) weather, fire or explosion; (c) war, terrorism, invasion, riot or other civil unrest; (d) governmental laws, orders, restrictions, actions, embargoes or blockades; (e) national or regional emergency; (f)injunctions, strikes, lockouts, labor trouble or other industrial disturbances; (g) shortage of adequate fuel, power, materials, or (h) any other event which is beyond the reasonable control of the affected party; provided that the party affected shall promptly notify the other of the force majeure condition and shall exert all commercially reasonable efforts to eliminate, cure or overcome any such causes and to resume performance of its obligations as soon as possible.

7.2.

Regulatory Compliance and Approval. After the Effective Date and during the Operational Transition Period, CORNERSTONE and Vansen shall cooperate to fulfill all responsibilities for regulatory compliance that either CORNERSTONE or Vansen may have with respect to the Product under applicable law and in accordance with the Asset Purchase Agreement and the Related Agreements. As soon as Vansen has received notification from FDA acknowledging the transfer of ownership of the Regulatory Files for the Product (but in no event later than April 1, 2012) (i) CORNERSTONE shall have no further responsibility for medical inquiries, regulatory submissions, pharmacovigilance, matters, including adverse experience reports, product complaints or reporting product liability claims regarding the Product.

7.3.

Regulatory Compliance - Adverse Event, Product Complaint Reporting and Recalls. During the Operational Transition Period, CORNERSTONE will be responsible for (i) managing Recall Procedures and (ii) filing adverse drug reaction reports with FDA and other applicable regulatory authorities for CORNERSTONE-branded Product sold by CORNERSTONE prior to the acknowledgment to Vansen by FDA with respect to the Regulatory Files as required by applicable laws and regulations including but not limited to ICH guidelines. In the event of a Recall during the Operational Transition Period, CORNERSTONE agrees that it will use commercially reasonable efforts to consult and work together with Vansen in determining a course of action to handle the Recall. Vansen will be responsible for (i) managing Recall Procedures and (ii) filing adverse drug reaction reports with FDA and other applicable regulatory authorities for Product after the Operational Transition Period. During the Operational Transition Period, each party shall provide, in writing to the other party, all information regarding adverse drug events and product complaints, immediately but no later than three (3) calendar days after becoming aware of such information, in the form and format received.

7.4.

Choice of Law. This Agreement, and all disputes arising out of or relating to this Agreement, or the performance, enforcement, breach or termination hereof or

thereof, and any remedies relating thereto, shall be construed, governed by and interpreted in accordance with the laws of the State of New York, without regard to the choice of Law principles thereof. Each Party consents to the exclusive jurisdiction of the Federal and State courts located in New York City, New York.

7.5.

Independent Contractor. The parties hereto are independent contractors. Nothing in this agreement is intended or shall be deemed to constitute a partnership, agency, franchise or joint venture relationship between the parties. Neither party shall enter into any agreements or make any commitments for the other.

7.6.

Confidentiality. The terms of the confidential disclosure agreement effective as of February 10, 2012 between Cornerstone and Vansen shall govern this Agreement

7.7.

Assignment. Neither party may assign or transfer this Agreement, in whole or in part, without the prior written consent of the other party, such consent not to be unreasonably withheld or delayed, except that either party may assign its rights and duties hereunder without obtaining such consent to any Affiliate. For greater certainty, the entering into by a party of any subcontracting, licensing or distributorship agreement shall not in itself constitute an assignment or transfer of this Agreement.

7.8.

Entire Agreement. This Agreement, together with the Asset Purchase Agreement and the Schedules attached hereto and thereto, constitutes the entire agreement between the parties hereto with respect to the subject matter hereof and except as expressly otherwise provided herein, supersedes and cancels all previous agreements, negotiations, commitments and writings in respect to the subject matter hereof.

7.9.

Successors and Assigns. The terms and conditions of this Agreement shall be binding upon and shall inure to the benefit of the parties hereto and their respective successors and permitted assigns.

7.10.

Modification and Waiver. No amendment, modification or alteration of the terms of this Agreement shall be binding unless the same shall be in writing and duly executed by the parties hereto, except that any of the terms or provisions of this Agreement may be waived in writing at any time by the party which is entitled to the benefits of such waived terms or provisions. No waiver of any of the provisions of this Agreement shall be deemed to or shall constitute a waiver of any other provision hereof (whether or not similar) and such waiver shall not be construed as a waiver or relinquishment, to any extent, of the right to assert or rely upon any such terms or conditions on any future occasion. No delay on the part of any party exercising any right, power or privilege hereunder shall operate as a waiver thereof.

7.11.

Notices. Notices under this Agreement shall be given in writing and shall be given by delivery in person, by electronic or facsimile transmission or other standard forms of written communications, by overnight courier or by registered or certified mail, postage prepaid:

If to Cornerstone:

Cornerstone Therapeutics Inc.

0000 Xxxxxxxx Xxxxx Xxxxx,

Xxxxx 000

Xxxx, XX 00000

Attention: General Counsel

If to Vansen:

Vansen Pharma, Inc.

0000-0000 xxxx. Xx Xxxxxxxxxxx X.,

Xxxxxxxxx, Xxxxxx,

XXXXXX, X0X 0X0

Attention: Xxxxxxx Xxxxxxxx, President

or at such other address for a party as shall be specified by like notice. The date of giving any such notice shall be the date of hand delivery, the date of confirmed receipt if sent by electronic or facsimile transmission, or other standard forms of written communications, the day after delivery to the overnight courier service, and the date three (3) calendar days following the posting of the registered or certified mail.

7.12.

Counterparts. This Agreement may be executed in two or more counterparts, each of which shall for all purposes be deemed an original and all of which shall constitute one and the same agreement.

7.13.

Survival of Certain Provisions. The terms, provisions, representations, and warranties contained in this Agreement that by their sense and context are intended to survive the performance thereof (including, without limitation, any payment obligations arising or accruing prior the completion of performance, expiration or termination of this Agreement) by either party or both parties hereunder shall so survive the completion of performance, expiration or termination of this Agreement.

7.14.

Severability. If any provision of this Agreement is held to be illegal, invalid or unenforceable under any present or future law, and if the rights or obligations of either party under this Agreement will not be materially and adversely affected thereby, (a) such provision will be fully severable, (b) this Agreement will be construed and enforced as if such illegal, invalid or unenforceable provision had never comprised a pan hereof, (c) the remaining provisions of this Agreement will remain in full force and effect and will not be affected by the illegal, invalid or unenforceable provision or by its severance herefrom, and (d) in lieu of such

illegal, invalid or unenforceable provision, there will be added automatically as a part of this Agreement a legal, valid and enforceable provision as similar to such illegal, invalid or unenforceable provision as may be possible and reasonably acceptable to the parties in order to accomplish, to the extent possible, the original business purpose and economic benefit of the original provision.

7.15.

Review by Legal Counsel. Each of the parties agrees that it has read and had the opportunity to review this Agreement with its legal counsel. Accordingly, the rule of construction that any ambiguity contained in this Agreement shall be construed against the drafting party shall not apply.

7.16.

Third Party Beneficiaries. Except as stated in Section 5.1 and 5.2, nothing in this Agreement, express or implied, is intended to confer upon any third party, any rights, remedies, obligations or liabilities.

7.17.

Cumulative Remedies. No remedy referred to in this Agreement is intended to be exclusive, but each shall be cumulative and in addition to any other remedy referred to in this Agreement or otherwise available under law or at equity.

7.18.

Further Assurances. Each party agrees to execute such further papers, agreements, documents, instruments and the like as may be necessary or desirable to effect the purpose of this Agreement and to carry out its provisions.

[REMAINDER OF PAGE INTENTIONALLY LEFT BLANK]

IN WITNESS WHEREOF, the undersigned have executed this Agreement as of the Effective Date.

VANSEN PHARMA INC.

CORNERSTONE THERAPEUTICS INC.

By:

/s/ Xxxxxxx Xxxxxxxx

By:

/s/ Xxxxxx Xxxxxx

Name:

Xxxxxxx Xxxxxxxx

Name:

Xxxxxx Xxxxxx

Title:

President

Title:

EVP

SCHEDULE 2.1

OPERATIONAL TRANSITION SERVICES

During the Operational Transition Period, Cornerstone will provide the services outlined below:

1.	Warehousing of the Products

2.	Customer service functions for the Products including communicating and transmitting orders to Vansen.

3.	Responding promptly to all product inquiries including adverse reactions and Recalls from FDA and customers regarding the Products,

4.	Regulatory, medical information and pharmacovigilance services.

5.	Quality assurance services in the same manner as prior to the Effective Date.

SCHEDULE 2.2

SALES FORCE TRANSITION SERVICES

During the Sales Force Transition Period, Cornerstone will continue to employ and manage a sales force of [***], [***] and [***] and will provide services including fleet, expense report management, PDMA compliance, payroll, benefits, SFA system management and administration of an incentive compensation plan consistent with Cornerstone’s past practices.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

EXHIBITS TO VANSEN APA


Exhibit E		Assignment and Assumption Agreement

ASSIGNMENT AND ASSUMPTION AGREEMENT

ASSIGNMENT AND ASSUMPTION AGREEMENT, entered into on March 7th, 2012 by Cornerstone Therapeutics Inc., a Delaware corporation (the “Seller”) and Vansen Pharma Inc, a Canadian corporation (the “Purchaser”).

WITNESSETH:

WHEREAS, the Purchaser and the Seller are parties to that certain Asset Purchase Agreement dated March 7, 2012 by and between Purchaser and Seller (the “Agreement”).

WHEREAS, pursuant to the Agreement, the Seller agreed to assign and the Purchaser agreed to assume certain contracts of the Seller, including:

A certain License and Supply Agreement entered into by and between Meiji Seika Kaisha, Ltd. and Cornerstone Biopharma, Inc. 10/12/2006 and the amendments thereto reflected by Amendment No. 1 effective 07/27/2007, and by Letter Agreements dated 07/27/2007 and 01/11/2008, and by an Addendum effective 08/14/2008 (the “Transferred Contract”)

WHERAS, with respect to such assignment and assumption of the Transferred Contract, Meiji Seika Pharma Co., Ltd., a successor to Meiji Seika Kaisha, Ltd. thereto and the Seller are wiling to revise certain terms and conditions provided for in the Transferred Contract and to execute a new contract (the “New Licensed and Supply Agreement”)

1. Effective from and after the effective date of the New License and Supply Agreement, the Seller hereby assigns to the Purchaser, free and clear of all Liens, the Transferred Contract.

2. Effective from and after the effective date of the New License and Supply Agreement, the Purchaser hereby assumes the Transferred Contract.

3. This Assignment and Assumption Agreement shall be construed and enforced in accordance with applicable federal law and the laws (other than the conflict law rules) of the State of New York.

4. In the event that any provision of this Assignment and Assumption Agreement is construed to conflict with a provision of the Agreement, the provision in the Agreement shall be deemed controlling.

5. This Assignment and Assumption Agreement shall bind and shall inure to the benefit of the respective parties and their assigns, transferees and successors.

IN WITNESS WHEREOF, the undersigned have executed this Assignment and Assumption Agreement as of the date first above written.


CORNERSTONE THERAPEUTICS INC. (as successor to Cornerstone Biopharma, Inc.)

By
		Name:
		Title:

PURCHASER

By
		Name:
		Title:

Consent is hereby given to this Assignment and Assumption by:

MEIJI SEIKA PHARMA CO., LTD. (as successor to Meiji Seika Kaisha, Ltd.)

By
		Name:
		Title:

EXHIBITS TO VANSEN APA


Exhibit F		Copromotion Agreement

COPROMOTION AGREEMENT

This COPROMOTION AGREEMENT (this “Agreement”) entered into and effective on March 7, 2012, (the “Effective Date”) by and among Vansen Pharma Inc. having a place of business at 0000-0000 xxxx. Xx Xxxxxxxxxxx X., Xxxxxxxxx (Xxxxxx), Xxxxxx, X0X 0X0 (“VANSEN”), and Cornerstone Therapeutics Inc., a Delaware corporation (“CORNERSTONE”), having a place of business at 0000 Xxxxxxxx Xxxxx Xxxxx, Xxxxx 000, Xxxx, XX 00000.

WHEREAS, CORNERSTONE develops, distributes, licenses and sells various pharmaceutical products, including the following: Zyflo CR (zileuton) Extended Release Tablets and Zyflo (zileuton) Tablets (the “Products”);

WHEREAS, VANSEN also develops, distributes, licenses and sells various pharmaceutical products; and

WHEREAS, CORNERSTONE has the exclusive rights, with rights to sublicense, in the United States of America to promote the Products; and

WHEREAS, the parties desire that VANSEN provide Representatives who will engage in Detailing (as hereinafter defined) of the Products on the terms and conditions of this Agreement.

NOW, THEREFORE, in consideration of the premises and intending to be legally bound hereby, the parties hereto agree as follows:

ARTICLE I

DEFINITIONS

1.1

Definitions. The following terms are used in multiple contexts in this Agreement and shall have the following meanings:

(a) “Affiliate” means any corporate or non-corporate business entity which controls, is controlled by, or is under common control with a party to this Agreement. A corporation or non-corporate business entity shall be regarded as in control of another corporation if it owns or directly or indirectly controls at least fifty percent (50%) of the voting stock of the other corporation, or (i) in the absence of the ownership of at least fifty percent (50%) of the voting stock of a corporation or (ii) in the case of a non-corporate business entity, if it possesses directly or indirectly, the power to direct or cause the direction of the management and policies of such corporation or non-corporate business entity, as applicable.

(b) “Applicable Laws” means all applicable statutes, ordinances, regulations, rules or orders of any kind whatsoever of any government authority or court of competent jurisdiction, including, without limitation, the Federal Food, Drug and Cosmetic Act (21 U.S.C. §301 et seq.), the Prescription Drug Marketing Act of 1987, Generic Drug Enforcement Act of 1992 (21 U.S.C. § 000x xx xxx.), xxx Xxxx-Xxxxxxxx Xxxxxxx (00 X.X.X. §0000x-0x et seq.), all as amended from time to time.

(c) “Detail” shall mean an interaction, face-to-face visit by a Representative with a Target, during which the following may be discussed: uses listed on the prescribing information, safety, effectiveness, contraindications, side effects, warnings and other relevant

characteristics of a Product by a Representative in a fair and balanced manner consistent with the requirements of the Applicable Laws, and using, as necessary or desirable, the Product Labeling and/or the Product Promotional Materials, and may include, at the discretion of Vansen, the provision of samples.

(d) “Product Labeling” means all labels and other written, printed, or graphic matter upon (i) any container or wrapper utilized with a Product, or (ii) any written material accompanying a Product, including, without limitation, product package inserts, all of which shall be provided by CORNERSTONE.

(e) “Product Promotional Materials” means all CORNERSTONE developed or CORNERSTONE approved written, printed or graphic material, including Product Labeling, intended for use by Representatives during a Detail, including visual aids, file cards, premium items, clinical studies, reprints, drug information updates and any other promotional support items that CORNERSTONE deems necessary to conduct the Program.

(f) “Program” means the program for Detailing of Product to be conducted by the Representatives under the direction and control of VANSEN during the term of this Agreement.

(g) “Representative” means an individual hired by or on behalf of VANSEN to conduct Details of Product in connection with the Program who shall be a full-time employee of and compensated by VANSEN, and whose activities in connection with the Program and Details shall be under the supervision, direction and control of VANSEN, and of whose time at least 30% shall be dedicated to Detailing the Products.

(h) “Target(s)” means a licensed health care provider within the Territory except for Pulmonary specialists identified and defined by IMS Health or another third party data vendor as either Pulmonary Critical Care Medicine or Pulmonary Disease Specialists and actually called upon by a Representative of VANSEN during the Initial Term.

(i) “Territory” means the United States of America

ARTICLE II

PROGRAM MANAGEMENT; GENERAL SCOPE OF ACTIVITIES

2.1 Program. VANSEN shall, within 30 days of signing this Agreement, design a Program that meets the approval of CORNERSTONE, which approval shall not be unreasonably withheld.

2.2 Representatives. VANSEN shall maintain a maximum of [***] trained Representatives who shall identify and Detail the Products to Targets in the Territory. The Representatives shall remain under the direct authority and control of the field sales management of VANSEN.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

2.3 Incentive Plan. The Program shall be linked to an incentive plan for which VANSEN will ensure that all the Representatives are be eligible. The target bonus payable to the Representatives and their managers under such plan shall be at least [***] of the total target bonus payable to such Representatives under the aggregate of all sales incentive plans in which they may at any time participate. Upon CORNERSTONE’s reasonable request VANSEN will provide a copy of any sales incentive plan and associated materials related to the Program to CORNERSTONE. CORNERSTONE may elect to create, communicate and provide compensation according to additional incentives such as per-prescription payments or sales contests for the Product. Such additional incentives would be in addition to the Initial Funding and Subsequent Detailing fees described below.

2.4 Communications; Quarterly Report. At least one (1) time per month, the designated project manager from each party shall convene via live person-to-person communication to discuss to discuss the Program. At the end of each calendar quarter, VANSEN will provide CORNERSTONE with a Quarterly Report including a summary of call activity made during the preceding quarter including such information as total call volume by territory and by product, number and percent of targets reached by territory and by product, frequency of targets reached by territory and by product, and utilization of sales materials and marketing programs by territory. VANSEN will also provide a list in database format of targets, whether called upon within the quarter or not, which includes unique descriptors, address, specialty, all names, the number of calls received each month within the quarter, and 12 months of TRx performance data per target (if available). VANSEN will also provide other such information relating to the Program as CORNERSTONE may reasonably from time to time request. CORNERSTONE may request upon receipt of the Quarterly Report, an in-person meeting with a location convenient to VANSEN to include the project manager from each party and the VANSEN employee directly responsible for sales, to review the Quarterly Report and discuss the Program.

2.5 Costs. Except as provided in Article 3 below, VANSEN shall be solely responsible for all costs associated with the Program.

2.6 Materials. VANSEN shall use only Product Promotional Materials provided by or purchased from CORNERSTONE. Under no circumstances shall VANSEN or the Representatives independently develop, create or use any other promotional material or literature for the Detailing of Product. All copyright and other intellectual property rights in Product Promotional Materials shall remain vested in CORNERSTONE.

2.7 Compliance. VANSEN shall instruct the Representatives to limit their statements and claims regarding each Product, including efficacy and safety, to those which are consistent with the Product Labeling and the Product Promotional Materials. The Representatives shall not add, delete or modify claims of efficacy or safety in the Detailing of any Product, nor make any changes (including underlining or otherwise highlighting any language or adding any notes thereto) in the Product Promotional Materials. The Representatives shall Detail the Products in adherence to PDMA, GMP and all applicable regulatory and professional requirements, and to all Applicable Laws.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

ARTICLE III

COMPENSATION

3.1 Initial Funding. Beginning on the Effective Date and ending March 31, 2013 (the “Initial Term” of the Agreement), [***]. Such amounts shall be payable within 30 days of receipt of VANSEN Quarterly Report.

3.2 Subsequent Detailing Fee. After the Initial Term, VANSEN will receive a detailing fee to be calculated using the definitions below, as follows:

Detailing Fee = [***]

The detailing fee shall be paid quarterly within thirty (30) days of receipt of VANSEN Quarterly Report. Payment shall be estimated from quarterly IMS Health or Wolters Kluwer source data, with [***] and [***] originating from the same source data.

3.3 Certain Definitions. For the purposes of calculating the above fees:

(a)

“Total Prescriptions” in any quarter means the number of prescriptions for Products written by all prescribers and pulled through the retail channel during such quarter.

(b)

“Net Sales” in any quarter means the gross amount received by CORNERSTONE for all bona fide sales of such Product to an unrelated third party (including any third party distributors for resale), less the following amounts actually incurred or accrued in accordance with U.S. generally accepted accounting principles applied in a consistent manner:

(i)

Credits or allowances granted for price adjustments of the Product;

(ii)

Normal and customary trade, quantity, and cash discounts actually allowed;

(iii)

Freight out, postage, shipping, insurance and other transportation charges to the extent included in the invoice price to a third party;

(iv)

Legally allowed chargebacks, rebates and fees or similar payments actually granted to customers, including, without limitation, pharmacy benefit management companies, health maintenance organizations, managed care organizations, federal, state, local and other governments, their agencies and purchasers and reimbursers;

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

(v)

Taxes, except for income, excise, ad valorem, franchise and property, or duties levied on, absorbed or otherwise imposed on such sale or performance, including value-added taxes, or other governmental charges otherwise imposed upon the billed amount, as adjusted for rebates and refunds, to the extent not paid by the Third Party.

(vi)

Launch discounts, stocking fees and other discounts extended to wholesalers, distributors, chain drug stores and other third party organizations who distribute the Product to pharmacies;

(vii)

Credit card processing charges and fees; and

solely to the extent the above deductions are taken in accordance with GAAP applicable to the particular selling entity.

Use of Product for promotional, sampling or compassionate use purposes or for use in clinical trials (but excluding post-approval clinical trials for which compensation is received by the selling entity) shall not be considered in determining Net Sales. In the case of any sale of Product between a party or its Affiliates or sublicensees for resale, Net Sales shall be calculated as above only on the first arm’s length sale thereafter to an unrelated third party.

A Net Sale shall be deemed to have been made upon the date such sale is so recorded in accordance with GAAP.

(c)

“[***]” in any quarter means [***]

(d)

“[***]” in any quarter means the number of [***] by all Targets and [***].

(e)

“[***]” means, with respect to any calendar quarter for which the detailing fee is being calculated, [***] of the number of [***] by all Targets and [***] during the same calendar quarter in the preceding year; and

(f)

“[***]” in any quarter means [***] minus [***].

3.4. Reconciliation. Within sixty (60) days after the end of each calendar year, CORNERSTONE shall reconcile the accruals for rebates, chargebacks, credits and allowances including those for distribution service agreements used in calculating quarterly payments against the actual amounts of such costs for such year. Any adjustments shall be made with (or deducted from) the next scheduled payment from CORNERSTONE.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

3.5 Payments. All payments due under this section shall be paid by wire transfer to the account specified in writing by VANSEN. At the time of payment, CORNERSTONE shall issue a written report to VANSEN clearly showing in reasonable detail the calculation of Net Sales.

3.6 Inspection Rights. Upon prior written notice and at mutually agreeable times, VANSEN shall have the right to inspect all CORNERSTONE’S financial information that is relevant to this agreement. The inspections shall be limited to no more than once during any calendar year during the Term of this agreement.

ARTICLE IV

OTHER UNDERSTANDINGS

4.1 VANSEN not authorized to Bind CORNERSTONE. Nothing in this Agreement shall be deemed to authorize VANSEN to act for, represent, or bind CORNERSTONE or any of its Affiliates other than as specifically provided by this Agreement.

4.2 Other VANSEN Activities. VANSEN shall not, during or for one year following the term of this Agreement, promote any product containing zileuton as an active ingredient. Except as specifically set forth herein, nothing in this Agreement shall in any way restrict or limit the commercial activities that VANSEN can undertake during the term of this Agreement and thereafter.

4.3 Program. VANSEN represents and warrants that it will at all times employ a sufficient number of Representatives to staff the Program, and that it will employ a sufficient number of supervisory staff and an administrative infrastructure to adequately train and monitor such Representatives.

4.4 Orders for Product. CORNERSTONE shall be exclusively responsible for accepting and filling purchase orders, billing, and returns with respect to the Products. If VANSEN or the Representatives receive orders for any Product, they shall transmit such orders to CORNERSTONE for acceptance or rejection, which acceptance or rejection shall be at CORNERSTONE’s sole discretion.

4.5 Product Updates. CORNERSTONE shall promptly inform VANSEN of any circumstance or change of circumstance that might affect the right of VANSEN to commercialize the Products in the Territory or interfere with VANSEN’ ability to perform and receive benefit under this Agreement.

4.6 Product Recall. In the event of a product recall, the parties agree to fully cooperate in such recall. CORNERSTONE shall be responsible at its own cost for implementing the recall and will reimburse VANSEN for costs incurred to provide such cooperation.

4.7 [***]

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

ARTICLE V

OMITTED

ARTICLE VI

INDEPENDENCE OF THE PARTIES

6.1 Independent Contractor. VANSEN is being retained and shall perform hereunder strictly as an “independent contractor.” Employees and Representatives of VANSEN performing services hereunder shall not be, and shall not be considered to be, employees of CORNERSTONE for any purpose and all Representatives shall be employees of VANSEN. Neither party shall have any responsibility for the hiring, termination, compensation, benefits or other conditions of employment of the other party’s employees except as otherwise provided in this Agreement.

6.2 No Joint Venture; Limited exclusivity. Nothing contained in this Agreement shall be construed as making the parties joint ventures or, except as otherwise provided herein, as granting to either party the authority to bind or contract any obligations in the name of or on the account of the other party or to make any guarantees or warranties on behalf of the other party. Nothing in this Agreement shall restrict CORNERSTONE from promoting or marketing any Product in any lawful manner it deems appropriate, directly or through third parties, except for Detailing in the Territory, which shall be restricted to VANSEN during the Term of the Agreement.

ARTICLE VII

TRAINING

7.1. Training Programs. VANSEN shall conduct under its exclusive direction and control home and/or classroom Product training for all Representatives and Directors on the Program. Such training shall include such medical and technical information and Product Promotional Materials about the Products that shall be provided by CORNERSTONE and such sales training relating to the Products shall represent at least a [***] focus on the Products (the “Training Program”) and coordinating the presentation of the Products with any other products in the Detail. CORNERSTONE shall reasonably assist VANSEN with the Training Program.

7.2 Continuing Education. The parties together agree to develop appropriate action plans to ensure that Representatives are kept continuously informed of all changes in Product Promotional Materials.

7.3 Training Materials and Promotional Materials. CORNERSTONE shall, within 30 days of singing this Agreement and thereafter as may be reasonably requested by VANSEN, deliver training materials and/or Product Promotional Materials to VANSEN or the Representatives.

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

ARTICLE VIII

COMMUNICATIONS

8.1 Communications from Third Parties. VANSEN and its Representatives shall communicate to CORNERSTONE all comments, statements, requests and inquiries of the medical profession or any other third parties relating to the Products that are out of the ordinary, or not covered by Product Labeling, of which VANSEN becomes aware. All responses to the medical profession or such other third parties shall be handled solely by CORNERSTONE. VANSEN shall provide reasonable assistance to CORNERSTONE to the extent requested by CORNERSTONE, and at CORNERSTONE’s sole cost and expense, to fully respond to such communications.

8.2 Government Agencies. All responses to government agencies concerning the Products shall be the sole responsibility of CORNERSTONE. VANSEN shall assist CORNERSTONE with respect to communications from government agencies to the extent requested by CORNERSTONE, at CORNERSTONE’s sole cost and expense. VANSEN shall use commercially reasonable efforts to assist CORNERSTONE to fully respond to such communications and be able to provide any and all forms, documents and related records to CORNERSTONE within 72 hours. VANSEN shall respond to any governmental agency subpoena directed to it concerning any Product, and shall be reimbursed by CORNERSTONE for all reasonable costs and expenses incurred, including, but not limited to, reasonable attorneys’ fees.

ARTICLE IX

INSURANCE

9.1 VANSEN Insurance Coverage Required. During the term of this Agreement, and with respect to liability hereunder for any post termination period during which a claim could be asserted against VANSEN, up to 5 years after termination, VANSEN shall maintain at its sole expense insurance coverage as follows:

Commercial General Liability insurance including with a combined single limit of [***], minimum liability of [***] each occurrence and [***] in the aggregate;

The foregoing insurance shall be maintained with responsible carriers and their terms of coverage shall be evidenced by certificates of insurance to be furnished by VANSEN to CORNERSTONE within 30 days of the date of this Agreement. Such certificates of insurance shall provide that at least 30 days’ written notice shall be given to CORNERSTONE prior to cancellation or modification of any of the material terms of coverage of any policy.

9.2 CORNERSTONE Insurance Coverage Required. CORNERSTONE shall maintain, at its sole expense, insurance coverage during the term of this Agreement, and with respect to liability hereunder for any post termination period during which a claim could be asserted against VANSEN, up to 5 years after termination, as follows:

(a) Product liability insurance with respect to the Products with coverage limits of not less than [***] per occurrence and [***] in the aggregate; and

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

(b) Commercial General Liability insurance including with a combined single limit of [***], minimum liability of [***] each occurrence and [***] in the aggregate;

All of the foregoing insurance shall be maintained with responsible carriers and their terms of coverage shall be as evidenced by certificates of insurance to be furnished by CORNERSTONE to VANSEN within 30 days of the date of this Agreement. Such certificates of insurance shall provide that at least 30 days’ written notice shall be given to VANSEN prior to cancellation or modification of any of the material terms of coverage of any policy.

ARTICLE X

ADVERSE REACTION REPORTING AND REGULATORY MATTERS

10.1 Immediate Notification. VANSEN agrees that it will notify CORNERSTONE as soon as reasonably practicable (but in no event after more than three days) of any information that VANSEN obtains through its Representatives concerning any Product or package complaint or any serious unexpected side effect, injury, toxicity, or sensitivity reaction or any unexpected incidence of severity thereof associated with the clinical uses, studies, investigations, tests and marketing of the Products, whether or not determined to be attributable to any Product. “Serious” as used in this Section 10.1 refers to an experience, which results in death, permanent or substantial disability, in-patient hospitalization, prolongation of existing in-patient hospitalization, or is a congenital anomaly, cancer, and the result of an overdose or life threatening. “Unexpected” as used in this Section 10.1 refers to (i) conditions or developments not previously submitted to governmental Agencies or encountered during clinical studies of the Product, and (ii) conditions or developments occurring with greater frequency, severity, or specificity than shown by information previously submitted to governmental Agencies or encountered during clinical studies of the Product. VANSEN shall notify CORNERSTONE in a timely manner (but in no event after more than three days) of any other adverse experience (i.e., any unfavorable and unintended change in the structure (signs), function (symptoms) or chemistry (laboratory data) of the body temporally associated with the use of the Product, whether or not considered related thereto. VANSEN and CORNERSTONE shall each issue appropriate instructions in their various Training Program and orientation sessions with Representatives with respect to the foregoing.

10.2 Threatened Agency Action. VANSEN shall immediately notify CORNERSTONE of any information VANSEN receives through its Representatives or otherwise regarding any threatened or pending action by a government agency which may affect any Product and VANSEN shall, at the request of CORNERSTONE and at the sole cost and expense of CORNERSTONE (including, without limitation, fees and expenses of counsel for VANSEN), cooperate with CORNERSTONE in formulating a procedure for taking appropriate action. In no event shall VANSEN itself respond to the government agency without the prior written consent of CORNERSTONE, unless VANSEN is compelled by law to respond even without

[***]

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.

CORNERSTONE’s written consent. VANSEN and CORNERSTONE shall each issue appropriate instructions in their various Training Program and orientation sessions with Representatives with respect to the foregoing.

ARTICLE XI

CONFIDENTIAL INFORMATION

11.1. Confidential Information. Each party acknowledges and agrees that it will have access to, or become acquainted with, Confidential Information of the other party in connection with the performance of the services required by this Agreement. For the purposes of this Agreement, “Confidential Information” shall mean any information of the disclosing party or any Affiliate thereof, which gives the disclosing party an advantage over its competitors who do not possess such information and constitutes valuable trade secrets and proprietary data which was revealed to the receiving party as a result of entering into or performing its obligations under this Agreement, including but not limited to, information which relates to Product, the Program, Health Care Providers, designs, methods, discoveries, improvements, documents, trade secrets, proprietary rights, business affairs, customer information or employee information. Confidential Information shall not include any information that:

(a) was known to the receiving party prior to the date of this Agreement, without an obligation to keep it confidential;

(b) was lawfully obtained by the receiving party from a third party without any obligation of confidentiality;

(d) becomes part of the public knowledge after disclosure by publication or otherwise except by breach of this Agreement;

(e) is developed by the receiving party independently by persons who did not have access to the Confidential information and apart from this Agreement.

(f) is otherwise knowledge possessed by the receiving party or its employees as the result of their industry experience or education.

The receiving party shall keep all Confidential Information in confidence and shall not, at any time during or for a period of five (5) years from the termination of this Agreement, without the disclosing party’s prior written consent, disclose or otherwise make available, directly or indirectly, any item of Confidential Information to anyone other than its employees and Representatives (and its legal counsel and consultants provided they are bound by similar obligations of confidentiality) who need to know the same in connection with fulfilling the purposes of this Agreement. The receiving party shall use the Confidential Information only in connection with fulfilling the purposes of this Agreement and for no other purpose. Each party shall inform its employees of the trade secret, proprietary and confidential nature of the Confidential Information.

11.2. Extraordinary Relief. In the event of the actual or threatened breach by the receiving party of any of the terms of this Article XI, the disclosing party shall have the right to

seek specific performance and injunctive relief, and, at the sole option of the disclosing party, the ADR provisions of Section 14.9 shall not be applicable. The rights granted by this paragraph are in addition to all other remedies and rights available at law or in equity.

ARTICLE XII

TERM AND TERMINATION

12.1 Effective Date. This Agreement shall take effect on the date on which both parties execute this Agreement, with the understanding that the Program shall continue in effect for twenty-four (24) months from that date, thereafter automatically renewing for successive twenty-four (24) month renewal periods unless either party provides the other party not less than sixty (60) days prior written notice of termination of the Agreement at the end of the then-current term; or, unless terminated earlier as set forth herein.

12.2 Bankruptcy; Insolvency. Either party may terminate this Agreement upon the occurrence of the following: (a) the entry of a decree or order for relief by a court having jurisdiction in the premises in respect of the other party in an involuntary case under the Federal Bankruptcy Code, as now constituted or hereafter amended, or any other applicable federal or state insolvency or other similar law and the continuance of any such decree or order unstayed and in effect for a period of sixty (60) consecutive days: or (b) the filing by the other party of a petition for relief under the Federal Bankruptcy Code, as now constituted or hereafter amended, or any other applicable federal or state insolvency or similar law.

12.3 Termination for Action by Competent Authority. In the event that either Party receives a notification by a government agency or any other competent authority requiring them to cease selling, marketing or promoting the Product, this Agreement shall be terminated effective as of the date required by such notification. At such time, VANSEN will provide written undertakings in whatever form CORNERSTONE may reasonably request, acknowledging and committing to comply with the terms of such written notification. If CORNERSTONE receives such undertakings, it shall, unless it is prohibited from doing so under terms of such notification, continue to pay to VANSEN all compensation, if any, pursuant to Section 3.1(a) that may be earned in the three (3) calendar months consisting of the month of termination and the two (2) succeeding months, less any outstanding payments due from VANSEN under Section 3.1(c), if any.

12.4 Termination for Cause. Either party may terminate this Agreement upon sixty (60) days’ prior written notice thereof to the other party upon the material breach by the other party of any of its representations, warranties, covenants or agreements contained in this Agreement. Upon the expiration of such notice period, this Agreement shall terminate without the need for further action by either party; provided, however, that if the breach upon which such notice of termination is based shall have been fully cured within such sixty (60) day period, then such notice of termination shall be deemed rescinded, and this Agreement shall continue in full force and effect, provided, however that a party shall not have the right to cure a material breach more than twice in any 24-month period. Such right of termination shall be in addition to such other rights and remedies as the terminating party may have under applicable law; provided further, however, that if CORNERSTONE fails to make any payment due hereunder within thirty (30) days of receipt of written notice from VANSEN regarding such overdue payment, VANSEN may either (i) immediately terminate this Agreement, or (ii) suspend services hereunder pending receipt of such payment; in each case concurrently with written notice to CORNERSTONE. If CORNERSTONE terminates this Agreement under this Section 12.4, CORNERSTONE shall pay VANSEN under Section 3.1 (a) through the last day of the month of the termination date, less any outstanding payments due from VANSEN under Section 3.1 (c).

12.5 Termination Without Cause. In addition to any other ground of termination, either party may terminate the Agreement at any time for any reason upon sixty (60) days advance notice to the other party at any time after the expiration of the Initial Term. If CORNERSTONE terminates this Agreement under this Section 12.5, then CORNERSTONE shall continue to pay to VANSEN all compensation, if any, pursuant to Section 3.1 (a) that may be earned in the three (3) calendar months consisting of the month of termination, less any outstanding payments due from VANSEN under Section 3.1 (c), if any, plus reimbursement for the buy-back of Product Samples at actual cost and shipping fees for return.

12.6 Termination; Return of Materials. Upon the request of CORNERSTONE, within sixty (60) days following the termination or expiration of this Agreement, VANSEN shall return to CORNERSTONE all Confidential Information, marketing plans, forms, territory lists, reports and any and all other tangible items provided to VANSEN by CORNERSTONE.

12.7 Reconciliation. Within six months after the expiration or earlier termination of this Agreement, CORNERSTONE shall reconcile the accruals for rebates, chargebacks, credits and allowances including those for distributor service agreements used in calculating quarterly payments under Section 3.1(a)(i) against the actual amounts of such costs for such year and provide VANSEN with the reconciliation report. Any adjustment shall be paid by CORNERSTONE or VANSEN within thirty (30) days after the delivery by CORNERSTONE of the reconciliation report.

12.8 Termination Due to Performance. In addition to any other ground of termination, Cornerstone may terminate the Agreement at any time if VANSEN is not able to grow sales of the Products above the established Baseline in year 2 of the Agreement.

12.9 Termination Due to Generic Entry. Either party may terminate this Agreement upon 10 days notice following the first commercial sale of a generic equivalent to any Zyflo Product. Following such a termination, CORNERSTONE will use its best efforts to complete a provisional reconciliation of, and pay, a reasonable estimate of all amounts due to VANSEN within 30 days, and to expedite the final reconciliation contemplated by Section 12.7 promptly thereafter.

ARTICLE XIII

INDEMNIFICATION

13.1 Indemnification by VANSEN. VANSEN shall defend, indemnify and hold CORNERSTONE, its Affiliates, directors, officers, employees and agents harmless from and against any and all claims, suits, actions, damages, assessments, interest charges, penalties, costs or expenses, including reasonable attorney’s fees (collectively, the “Indemnified Amounts,”) arising out of (a) the material breach by VANSEN of any of its obligations, representations or warranties under this Agreement, including, without limitation, VANSEN’s failure to comply with its obligations pertaining to employment of Program Personnel, (b) a negligent or willful act or omission on the part of VANSEN (including any Representative or Director), (c) any federal or state claims or assessment for nonpayment or late payment by VANSEN of any tax or contribution based on compensation or other benefits owed to any of

the VANSEN Representatives, including, without limitation, a claim or assessment that CORNERSTONE should have withheld any amounts related thereto, (d) requests by VANSEN or by third parties (in connection with a claim against VANSEN) pursuant to a subpoena or court order for the production by CORNERSTONE of documents or any other materials relating to the Program or to interview, depose and/or elicit testimony from CORNERSTONE employees regarding the Program, (e) any violation by VANSEN of any and all Applicable Laws of any governmental body having jurisdiction over the exercise of rights under this Agreement, or (f) any misuse or misappropriation of Product samples distributed by VANSEN.

13.2 Indemnification by CORNERSTONE. Subject to the extent of any indemnification from VANSEN pursuant to Section 13.1 hereof, CORNERSTONE shall defend, indemnify and hold VANSEN, its Affiliates, directors, officers, employees and agents harmless from and against any and all Indemnified Amounts arising out of (a) the material breach by CORNERSTONE of any of its obligations under this Agreement, (b) a negligent or willful act or omission on the part of CORNERSTONE, (c) the manufacture, use, or sale of Product or a manufacturing design or defect of Product or a claim arising out of CORNERSTONE’s failure to warn, (d) any marketing or Product Promotional Materials provided to VANSEN by CORNERSTONE, (e) any claims by any third party that VANSEN’s promotion of any Products or the manufacture, sale or use of Product infringes or violates any license, patent, copyright, trademark or other intellectual property right of that third party, (f) any negligent or willful acts or omissions on the part of CORNERSTONE with respect to Representatives or other VANSEN employees or those individuals who have made application to be Representatives of VANSEN, (g) requests by CORNERSTONE or by third parties (in connection with a claim against CORNERSTONE) pursuant to a subpoena or court order for the production by VANSEN of documents or other materials relating to the Program or to interview, depose and/or elicit testimony from VANSEN employees, including Program Personnel, regarding the Program.

13.3 Indemnification Procedures. A Person seeking indemnification under this Article XII (the “Indemnified Party”) shall give the indemnifying party (the “Indemnifying Party”) prompt written notice of any action, claim, demand, discovery of fact, proceeding or suit for which indemnification is sought (a “Claim”); provided, however, that the failure of an Indemnified Party to give such prompt notice shall not reduce the Indemnifying Party’s obligations under this Article XII except to the extent that the Indemnifying Party’s defense of any such matter is actually prejudiced thereby. The Indemnifying Party shall indemnify the Indemnified Party for its defense and/or representation with respect to the Claim. In the event such a defense and/or representation are required, the Indemnifying Party agrees that it will immediately confer with the Indemnified Party in order to reach an agreement on the terms and conditions of any such defense (the “Defense Agreement”). Such agreement shall include, but not be limited to: (i) the choice of counsel; (ii) the defense strategy to be undertaken; (iii) settlement strategies and issues; (iv) manner and method of document productions; (v) presentation of employees as witnesses; (vi) the retention of consultants and expert witnesses; and (vii) trial and appellate strategy. In the event of a material disagreement, the Indemnifying Party shall have the right to make the final determination regarding the defense. The Indemnifying Party shall not settle any Claim without the prior written consent of the Indemnified Party, which consent shall not be unreasonably withheld or delayed. Any such settlement shall, unless the Indemnified Party agrees in writing to the contrary, be conditioned on: (i) dismissal with prejudice of all claims pending or which may be brought in the future against the Indemnified Party; (ii) an express provision that there is no admission or acknowledgement of liability on the part of the Indemnified Party; and (iii) an express provision that the terms of any such settlement be treated as confidential. If the Indemnifying Party is unable to settle any such claims on behalf of the Indemnified Party in this manner, then the Indemnifying Party shall continue to fully defend and indemnify the Indemnified Party pursuant to the terms of this Agreement and the Defense Agreement.

ARTICLE XIV

MISCELLANEOUS

14.1. No Waiver; Cumulative Remedies. No failure or delay on the part of either party in exercising any right, power or remedy hereunder shall operate as a waiver thereof; nor shall any single or partial exercise of any such right, power or remedy preclude any other or further exercise thereof or the exercise of any other right, power or remedy hereunder. No waiver of any provision hereof shall be effective unless the same shall be in writing and signed by the party giving such waiver. The remedies herein provided are cumulative and not exclusive of any remedies provided by law.

14.2 Headings. Article and Section headings used in this Agreement are for convenience only and shall not affect the construction of this Agreement.

14.3 Governing Law; Jurisdiction. This Agreement shall be construed and the respective rights of the parties hereto determined according to the substantive laws of the State of New York notwithstanding the provisions governing conflict of laws under such law to the contrary.

14.4 Severability. If any provision of this Agreement or any other document delivered under this Agreement is prohibited or unenforceable in any jurisdiction, it shall be ineffective in such jurisdiction only to the extent of such prohibition or unenforceability, and such prohibition or unenforceability shall not invalidate the balance of such provision to the extent it is not prohibited or unenforceable nor the remaining provisions hereof, nor render unenforceable such provision in any other jurisdiction. In the event any provisions of this Agreement shall be held to be invalid, illegal or unenforceable, the parties hereto shall use their best efforts to substitute a valid, legal and enforceable provision which, insofar as practical, implements the purposes hereof.

14.5 Entire Agreement; Modification. This Agreement contains the entire agreement between the parties in respect of the subject matter hereof and supersedes and cancels all previous agreements, negotiations, commitments and writings between the parties hereto in respect of the subject matter hereof and may not be changed or modified in any manner or released, discharged, abandoned or otherwise terminated unless in writing and signed by the duly authorized officers or representatives of the parties.

14.6 Notices. Any notice or request required or permitted to be given in connection with this Agreement shall be deemed to have been sufficiently given if sent by pre-paid registered or certified mail or facsimile transmission to the intended recipient at the address set forth below or such other address as may have been furnished in writing by the intended recipient to the sender. The date of mailing or facsimile transmission shall be deemed to be the effective date on which notice was given, provided that all facsimile transmissions shall contain a provision requiring the intended recipient to confirm receipt and such facsimile transmissions shall not be effective unless confirmation of its receipt is received within twenty-four hours of its transmission.

Any notice required to be given shall be addressed:


If to VANSEN, to:		Vansen Pharma, Inc.
		0000-0000 xxxx. Xx Xxxxxxxxxxx X.,
		Xxxxxxxxx, Xxxxxx,
		XXXXXX, X0X 0X0

		Attention: Xxxxxxx Xxxxxxxx, President


If to CORNERSTONE, to:
		Cornerstone Therapeutics Inc.
		0000 Xxxxxxxx Xxxxx Xxxxx, Xxxxx 000
		Xxxx, XX 00000

		Attention: President

14.7 Execution in Counterparts. This Agreement may be executed in counterparts, each of which, when executed and delivered, shall be deemed to be an original and all of which together shall constitute one and the same document.

14.8 Assignment. Except as otherwise expressly provided in this Section 14.8, neither party shall assign this Agreement in whole or in part without the prior written approval of the other party (such approval not to be unreasonably withheld or delayed). Any such attempted assignment without prior written consent shall be void and ineffective. Notwithstanding the foregoing, either party may, without the other party’s consent, assign its right, title and interest in this Agreement to any entity with which it may merge or consolidate, which acquires all or greater than fifty percent (50%) of its business and assets, or which otherwise controls, is controlled by or is under common control with the assigning party. This Agreement and the rights and obligations granted and undertaken hereunder shall be binding upon and inure to the benefit of the parties hereto, and their successors, trustee(s) or receiver(s) in bankruptcy and permitted assigns.

14.9 Dispute Resolution.

(a) If a dispute arises between the parties in connection with this Agreement or any document or instrument delivered in connection herewith, including without limitation, an alleged breach of any representation, warranty or covenant herein or therein, or a disagreement regarding the interpretation of any provision hereof or thereof (a “Dispute”), the parties shall use the following procedure in good faith prior to any party pursuing other available judicial or nonjudicial remedies:

(b) A meeting shall be held between the parties within ten days after any party gives written notice of a Dispute to the other party (the “Dispute Notice”). The meeting shall be attended by a representative of each party having decision-making authority regarding the Dispute (subject to Board of Directors’ or equivalent approval, if required), to attempt in good faith to negotiate a resolution of the Dispute.

(c) If, within thirty days after the Dispute Notice, the parties have not succeeded in negotiating a written resolution of the Dispute, upon written request by any party to the other party to this Agreement, the parties shall promptly negotiate in good faith to jointly appoint a mutually acceptable neutral person not affiliated with any of the parties (the “Neutral”). If the parties so agree in writing, a panel of two or more individuals (such panel also being referred to as the “Neutral”) may be selected by the parties. The fees and costs of the Neutral shall be shared equally between the parties.

(d) In consultation with the Neutral, the parties shall negotiate in good faith to select or devise a nonbinding alternative dispute resolution procedure (“ADR”) by which they will attempt to resolve the Dispute, and a time and place for the ADR to be held, with the Neutral (at the written request of any party to the other party) making the decision as to the procedure, place and time if the parties have been unable to agree on any such matters in writing within ten days after selection of the Neutral.

(e) The parties shall participate in good faith in the ADR to its conclusion; provided, however, that no party shall be obligated to continue to participate in the ADR if the parties have not resolved the Dispute in writing within 60 days after the Dispute Notice and either party shall have terminated the ADR by delivery of written notice of termination to the other party following expiration of the 60 days. Following any such termination notice after selection of the Neutral and if any party so requests in writing to the Neutral (with a copy to the other party), then the Neutral shall make a recommended resolution of the Dispute in writing to each party, which recommendation shall not be binding upon the parties; provided, however, that the parties shall give good faith consideration to the settlement of the Dispute on the basis of such recommendation.

(f) Notwithstanding anything herein to the contrary, nothing in this Section 14.9 shall preclude either party from (a) seeking interim or provisional relief, in the form of a temporary restraining order, preliminary injunction or other interim equitable relief concerning a Dispute either prior to or during the ADR if necessary to protect the interests of such party or (b) terminating this Agreement in accordance with Article XII. This Section 14.9 otherwise shall be enforceable in accordance with its terms.

14.10 Public Announcements. Any public announcements or similar publicity with respect to this Agreement or the transaction contemplated herein shall be at such time and in such manner as the parties shall mutually agree, provided that nothing herein shall prevent either party from, upon notice to and opportunity to review by the other, making such public announcements as such party’s legal obligations require.

14.11 Maintenance of Records. VANSEN and CORNERSTONE each agree that throughout the duration of this Agreement and for a period of six years after the termination of this Agreement each will maintain records and otherwise establish procedures to assure compliance with all regulatory, professional, and other applicable legal requirements which relate to the Detailing and marketing of the Products and if applicable, with the other services and activities to be performed hereunder.

14.12 Force Majeure. Failure of either party hereto to fulfill or perform its obligations under this Agreement shall not subject such party to any liability if such failure is caused or occasioned by, without limitation, acts of God, acts of terrorism, fire, explosion, flood, drought, war, riot, sabotage, embargo, strikes or other labor disputes (which strikes or disputes need not be settled), compliance with any order, regulation, or request of government, or by any other

event or circumstance of like or different character to the foregoing beyond the reasonable control and without the fault or negligence of such party, (a “Force Majeure Event”) provided such party uses reasonable efforts to remove such Force Majeure Event and gives the other party prompt notice of the existence of such Force Majeure Event. If a Force Majeure Event causes VANSEN to fail to meet its obligations under Section 2.1 for two consecutive months, then CORNERSTONE may terminate this Agreement on thirty (30) days notice in which case the Agreement shall be deemed terminated pursuant to Section 12.1.

14.13 Survival. The provisions of Articles III (compensation), IX (insurance), XI (confidential information), 12.7, XIII (indemnification) and XIV (miscellaneous) shall survive the termination of this Agreement.

14.14 No Third Party Beneficiaries. This Agreement shall be binding upon and inure solely to the benefit of the parties hereto and their permitted assigns and nothing herein, express or implied, is intended to or shall confer upon any other person, any legal or equitable right, benefit or remedy of any nature whatsoever under or by reason of this Agreement.

IN WITNESS WHEREOF, the parties have caused this Agreement to be executed by their duly authorized officers.


CORNERSTONE THERAPEUTICS INC.		VANSEN PHARMA INC.

By:	/s/ Xxxxxx Xxxxxx	By:	/s/ Xxxxxxx Xxxxxxxx

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ASSET PURCHASE AGREEMENT

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