FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 69097-459 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameFENOFIBRATE
Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208709
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20161215
Package count2

External sources

Source: openFDA. Public-domain (CC0).