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TERBINAFINE HYDROCHLORIDE

NDC 68071-2381 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameTerbinafine Tablets 250 mg
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077137
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20210108
Package count1

External sources

Source: openFDA. Public-domain (CC0).