FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 71335-0891 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA208709
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20161215
Package count3

External sources

Source: openFDA. Public-domain (CC0).