FDA NDC Directory · JSON-LD · Markdown

TERBINAFINE

NDC 72189-243 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / Manufacturerdirect rx
Marketing categoryAbbreviated NDA (generic) · App ANDA078297
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20210723
Package count1

External sources

Source: openFDA. Public-domain (CC0).