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Perampanel

NDC 0480-7063 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209801
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPERAMPANEL (4 mg/1)
Marketing started20250529
Package count1

External sources

Source: openFDA. Public-domain (CC0).