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[Duchamp's ready-made pharmaceutical ampoule]

Thierry Lefebvre1

  • 1CCI, UFR de Biologic, Université Paris VII-Denis Diderot, 2 place Jussieu, 75251 Paris cedex 05.

Revue D'Histoire De La Pharmacie
|December 13, 2006
PubMed

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Pharmaceutical Equivalents01:26

Pharmaceutical Equivalents

As defined by regulatory standards, pharmaceutical equivalents require generic drug products to have identical dosage forms and chemically identical active pharmaceutical ingredients (APIs). They must adhere to compendial or applicable standards for potency, content uniformity, disintegration times, and dissolution rates. In the case of modified-release dosage forms, variations in drug content are permissible as long as the delivered amount remains consistent with the innovator drug product.