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Terbinafine

NDC 71335-1124 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameTerbinafine Hydrochloride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA078297
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20070702
Package count9

External sources

Source: openFDA. Public-domain (CC0).