FDA NDC Directory · JSON-LD · Markdown

Terbinafine

NDC 71205-152 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077533
Dosage form / routeTABLET · ORAL
Active ingredientsTERBINAFINE HYDROCHLORIDE (250 1/1)
Marketing started20160627
Package count6

External sources

Source: openFDA. Public-domain (CC0).