FDA NDC Directory · JSON-LD · Markdown

TERBINAFINE

NDC 87564-010 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameterbinafine hydrochloride tablet
Labeler / ManufacturerAmerisyn LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076390
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20260803
Package count2

External sources

Source: openFDA. Public-domain (CC0).