FDA NDC Directory · JSON-LD · Markdown

TERBINAFINE HYDROCHLORIDE

NDC 69097-731 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameTerbinafine Tablets 250 mg
Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077137
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20210108
Package count2

External sources

Source: openFDA. Public-domain (CC0).