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Vigabatrin

NDC 59651-367 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA215601
Dosage form / routeTABLET · ORAL
Active ingredientsVIGABATRIN (500 mg/1)
Marketing started20220510
Package count1

External sources

Source: openFDA. Public-domain (CC0).