FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 51655-009 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076509
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20140507
Package count1

External sources

Source: openFDA. Public-domain (CC0).