FDA NDC Directory · JSON-LD · Markdown

Terbinafine

NDC 50090-3575 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameTerbinafine Hydrochloride
Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA078297
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 mg/1)
Marketing started20070702
Package count2

External sources

Source: openFDA. Public-domain (CC0).