FDA NDC Directory · JSON-LD · Markdown

Banzel

NDC 62856-582 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namerufinamide
Labeler / ManufacturerEisai Inc.
Marketing categoryNew Drug Application (innovator) · App NDA021911
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRUFINAMIDE (200 mg/1)
Marketing started20081114
Package count2

External sources

Source: openFDA. Public-domain (CC0).