FDA NDC Directory · JSON-LD · Markdown

Terbinafine Hydrochloride

NDC 68071-1640 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077137
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20140813
Package count1

External sources

Source: openFDA. Public-domain (CC0).