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Felbamate

NDC 72578-056 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerViona Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA208970
Dosage form / routeTABLET · ORAL
Active ingredientsFELBAMATE (400 mg/1)
Marketing started20200303
Package count5

External sources

Source: openFDA. Public-domain (CC0).