Generic Drugs definition
Generic Drugs means any product containing compound that (i) is defined in a particular country in the Territory as a generic drug to the Compound by applicable legal texts or governing health authorities in such country, or (ii) can be substituted for the Compound by a pharmacy, other than a product introduced in such country by INDEVUS, its Affiliates or INDEVUS Sublicensees.
Generic Drugs means non-brand drugs (including specialty drugs and therapeutic biological products), sold at a lower cost than the equivalent brand. A generic drug is the therapeutic equivalent of a brand name drug, i.e., it contains the same active ingredients and is identical in strength, concentration, and dosage form.
Generic Drugs means any product containing Compound for which Registration is obtained by an abbreviated NDA (“ANDA”) or other abridged procedure in the United States or a corresponding application in any country of the LICENSEE Territory, other than a Product introduced in such country by LICENSEE, its Affiliates or its sublicensees.
Examples of Generic Drugs in a sentence
The Copayment for Formulary Generic Drugs is shown in the Summary of Benefits.
Generic Drugs are listed on the Drug List which is available on the Blue Cross and Blue Shield of Montana website at ▇▇▇▇▇://▇▇▇.▇▇▇▇▇▇.▇▇▇/rx-drugs/drug-lists/drug-lists.
Available Prescription Drug Products include Brand-Name Drugs and Generic Drugs.
If not otherwise excluded, the Formulary includes all Generic Drugs.
The Copayment for Mail Ser- vice Generic Drugs is shown in the Summary of Benefits.
More Definitions of Generic Drugs
Generic Drugs means products submitted or approved pursuant to an ANDA or Section 505(b)(2) of the FDCA (and any applicable foreign marketing authorizations) which are marketed or in development to be marketed as generic products.
Generic Drugs means a drug that, in comparison with an Innovative Drug, contains identical amounts of the identical medicinal ingredients, in comparable dosage forms, but does not necessarily contain the same non- medicinal ingredients and which is interchangeable with the said Innovative Drug.
Generic Drugs means any product containing Compound for which Regulatory Approval for the same indication(s) as that of the Product is obtained by ANDA in the United States or a corresponding application in any country other than United States in the MN Territory; in each case other than a product introduced in such country by MN, its Affiliates or sublicensees.
Generic Drugs means all drugs that are not defined as “Brand Drugs.”
Generic Drugs means Drugs or substances which:
Generic Drugs means any pharmaceutical composition containing the same Compound as contained in Product Sold by MN, an MN Affiliate and/or an MN Sublicensee, in each case other than Product introduced in such country or jurisdiction by MN, an MN Affiliate and/or an MN Sublicensee.
Generic Drugs based on the definitions contained in this Agreement, and shall include all Dispensed Claims for Covered Items, including, if they are Covered Items, all insulin supplies, all test strips and insulin products, but excluding all (i) coded and uncoded Compound Drugs; (ii) drugs dispensed at the Specialty Drug Pharmacy; (iii) Claims from LTC pharmacies or government owned or operated pharmacies (e.g. Veterans Administration); (iv) Claims paid at government required amounts (e.g. Medicaid); (v) 340B Claims; (vi) vaccines; and (vii) Claims paid through another insurer as a result of the coordination of benefits. PBM shall include all Dispensed Claims described as being “included” in this paragraph, regardless of whether PBM reimbursed a pharmacy using an AWP discount price, a MAC price or a non-MAC price or U&C; In instances where PBM used U&C to reimburse the retail pharmacy, PBM will be entitled to credit itself with a $0 Dispensing Fee, as described in the Definition for Dispensing Fee.