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Banzel

NDC 75929-098 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namerufinamide
Labeler / ManufacturerPharma Packaging Solutions, LLC dba Tjoapack LLC
Marketing categoryNew Drug Application (innovator) · App NDA021911
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRUFINAMIDE (400 mg/1)
Marketing started20081114
Package count2

External sources

Source: openFDA. Public-domain (CC0).