FDA NDC Directory · JSON-LD · Markdown

Terbinafine

NDC 76282-209 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerExelan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077533
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20120425
Package count3

External sources

Source: openFDA. Public-domain (CC0).