FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 50268-313 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA076509
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20150813
Package count1

External sources

Source: openFDA. Public-domain (CC0).