FDA NDC Directory · JSON-LD · Markdown

Felbamate

NDC 70771-1077 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208970
Dosage form / routeTABLET · ORAL
Active ingredientsFELBAMATE (400 mg/1)
Marketing started20170815
Package count5

External sources

Source: openFDA. Public-domain (CC0).