Generic Equivalence

Définition

The demonstration that a generic drug delivers the same amount of active ingredient to the bloodstream at the same rate as the brand-name product. The FDA requires generic drugs to have an AUC and Cmax within 80-125% of the reference drug to be considered bioequivalent.

Exemple

Generic omeprazole must demonstrate that its absorption profile is within the 80-125% bioequivalence window of brand Prilosec.

Termes Associés

Peak Plasma Concentration Cmax Area Under the Curve AUC Generic Drug

Mentionné dans les Guides

Generic vs. Brand Name Drugs

Generic drugs contain the same active ingredient as their brand-name counterparts and must meet rigorous FDA standards. Understanding how generics …
Generic Drugs: Safety, Savings, and Myths

Generics account for over 90% of US prescriptions yet cost a fraction of brand-name drugs. This guide explains FDA bioequivalence …
Biosimilar Drugs: Affordable Biologics

Biologics revolutionized treatment for cancer, autoimmune disease, and diabetes, but their cost can be prohibitive. Biosimilars offer comparable effectiveness at …