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brivaracetam

NDC 70771-1756 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214501
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBRIVARACETAM (50 mg/1)
Marketing started20260221
Package count3

External sources

Source: openFDA. Public-domain (CC0).