Prescription Product definition

Prescription Product means, in respect of any jurisdiction, any oral care, nutritional care, skin care or other cosmetic or healthcare product or device of any kind, in each case, for the treatment of, or use by, human beings, which is (i) only available with a prescription, or (ii) available without, or both with and without, a prescription but is subject to the same regulatory classification and/or regulatory treatment (including in relation to advertising) as a product or device that is only available with a prescription;
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Prescription Product means any prescription drug or device, including any controlled substance, as those terms are defined in Iowa Code section 155A.3.
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Prescription Product means any therapeutic product or therapeutic treatment that generally requires a prescription by a Licensed Healthcare Practitioner under applicable laws or regulations or is eligible for reimbursement by a governmental body or a health care provider only if prescribed by a Licensed Healthcare Practitioner.
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Examples of Prescription Product in a sentence

  • Pharmacy Prescription Product: ZYDELIG Dose:150 mg taken orally, twice daily100 mg taken orally, twice dailyLine of Therapy:2L 3L 4LOther: Quantity: Day Supply: Refills: Diagnosis (ICD-10 code): Patients experiencing insurance delays of greater than 5 days may be eligible for QuickStart.

  • Medical Prescription (Rx)A Medical Prescription Product (Rx) (often referred to as a Pharmaceutical) is a drug, medical device, or medicinal specialty that requires a medical prescription or direct medical intervention.

  • Cupp Jr., Preemption’s Rise (and Bit of a Fall) as Products Liability Reform: Wyeth, Riegel, Altria, and the Restatement (Third)’s Prescription Product Design Defect Standard, 74 BROOK.

  • First Prescription Product Launched in the USAIn July of 2011, Skinvisible’s licensee, Women's Choice Pharmaceuticals LLC (Gilbert, Arizona) launched ProCort®, Skinvisible's first prescription product in the United States.

  • Subject to the terms of this Addendum, Company agrees to pay Retailer a volume rebate (“High Volume Rebate”) equal to [*]% of Retailer’s Net Qualified Prescription Product Purchases (as defined below) during each calendar year (or portion thereof) under the Rx Program Agreement after the Addendum Effective Date.

  • Effective November 27, 2019 returned Prescription Product must also include the original invoice number in order to be Saleable, in Compliance with the Drug Supply Chain Security Act.

  • Cupp Jr., Preemption's Rise (and Bit of a Fall) as Products Liability Reform: Wyeth , Riegel , Altria, and the Restatement (Third) 's Prescription Product Design Defect Standard, 74 BROOK.

  • Schering intends to source its supply of omeprazole and of Licensed Products in finished form from the same sources as referenced by Santarus in its NDA for the applicable Prescription Product.

  • When applied correctly, markup pricing practices constitute a practical rule-of-thumb approach to setting prices that ensure MR = MC for each relevant product or product class.

  • In order to be eligible for the High Volume Rebate, ( i ) the actual Net Qualified Prescription Product Purchases for such calendar year (or portion thereof in which Retailer participated in the Rx Program Agreement after the Addendum Effective Date) must equal or exceed $[*] ([*] dollars) and (ii) the Retailer must be in compliance with Section 1 of the Rx Program Agreement.


More Definitions of Prescription Product

Prescription Product means a Product subject to the provisions of Section 503 (b) 1 (B) of the Act.
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Prescription Product for a Licensed Product in a country means such product cannot be sold to a consumer without a prescription from a licensed healthcare practitioner in such country.
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Prescription Product for a Licensed Product in a country means such product cannot be sold to a consumer without a prescription from a licensed healthcare practitioner in such country. 1.36 “Regulatory Approval” in a particular country means all approvals (including any applicable governmental price and reimbursement approvals), licenses, registrations, and authorizations of any federal, national, multinational, state, provincial or local Regulatory Authority, department, bureau and other governmental entity that are necessary for the marketing and sale of a Licensed Product in a country. 1.37 “Regulatory Authority” means any applicable governmental authority responsible for granting Regulatory Approvals or pricing approvals for Licensed Products, including the FDA, the European Medicines Agency and any corresponding national or regional regulatory authorities. 1.38 “Regulatory Materials” means any regulatory application, submission, notification, communication, correspondence, registrations, approvals and other filings made to or received from a Regulatory Authority relating to any Licensed Product, including, without limitation, INADs, INDs clinical trial applications, NADAs, NDAs and any other marketing authorizations. 1.39 “Regulatory Materials Receipt” means the date on which Elanco provides Tarsus with the Regulatory Materials in existence as of the Effective Date that are reasonably necessary to research, develop, make, use or otherwise exploit Licensed Products in the Field in the Territory. Such materials include, without limitation, [***], FDA approval letter, and FDA correspondence related to 21Sep18 Safety Communication. 1.40 “Restated Certificate” means Tarsus’ Amended and Restated Certificate of Incorporation on file with the Secretary of State of the State of Delaware. 1.41 “Royalty Term” means, with respect to any Licensed Product in a given country, the period of time commencing on the date of the First Commercial Sale of such Licensed Product in such country and ending on the latest of: (a) expiry of the last-to-expire of the Licensed Patents which has at least one (1) Valid Claim Covering such Licensed Product in such country; (b) the expiration of regulatory exclusivity for such Licensed Product in such country; and (c) ten (10) years after first commercial sale of such Licensed Product in such country. 1.42 “SEC” means the U.S. Securities and Exchange Commission.
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Prescription Product means any product which requires approval or registration of the product as a prescription therapeutic or prophylactic drug by the U.S. FDA, or comparable regulatory authority in any other country, before it can be used by, or marketed to, or sold to consumers.
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Related to Prescription Product

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Therapeutic Product means a health product categorised as a therapeutic product in the First Schedule to the Act;

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • Diagnostic Product means any test or assay for diagnosing or detecting a disease, disorder, medical condition, or symptom.

  • Licensed Product means a product or part of a product in the Licensed Field of Use: (A) the making, using, importing or selling of which, absent this license, infringes, induces infringement, or contributes to infringement of a Licensed Patent; or (B) which is made with, uses or incorporates any Technology.

  • Collaboration Product means a pharmaceutical product containing or comprising Compound in any dosage form alone, or in combination with, one or more other pharmaceutically active ingredients, and any and all Improvements thereto.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • cosmetic product means any substance or mixture intended to be placed in contact with the external parts of the human body (epi­ dermis, hair system, nails, lips and external genital organs) or with the teeth and the mucous membranes of the oral cavity with a view exclusively or mainly to cleaning them, perfuming them, changing their appearance, protecting them, keeping them in good condition or correcting body odours;

  • Aerosol Product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • Approved Product means any water fitting, plumbing product, material or component which is the subject of an existing WRAS Approval;

  • Nicotine product means a product that contains nicotine and is not any of the following:

  • Licensed Products means tangible materials which, in the course of manufacture, use, sale, or importation, would be within the scope of one or more claims of the Licensed Patent Rights that have not been held unpatentable, invalid or unenforceable by an unappealed or unappealable judgment of a court of competent jurisdiction.

  • Hemp product means the same as that term is defined in § 3.2-4112.

  • complex product means a product which is composed of multiple components which can be replaced permitting disassembly and re-assembly of the product.

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Final Product means a reasonably homogenous cannabis product in its final packaged form created using the same standard operating procedures and the same formulation.

  • Royalty Product means, either (a) an Alnylam Royalty Product, or (b) an Inex Royalty Product.

  • Participating Product means any of the Breville products listed in the table below by model name and number that are supplied by Breville in Australia and sold directly by Breville or by a Participating Retail Store:

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Cannabis product means cannabis that has undergone a process whereby the plant material has been transformed into a concentrate, including, but not limited to, concentrated cannabis, or an edible or topical product containing cannabis or concentrated cannabis and other ingredients.