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Rufinamide

NDC 0054-0425 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204988
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRUFINAMIDE (200 mg/1)
Marketing started20210530
Package count1

External sources

Source: openFDA. Public-domain (CC0).