FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 0115-5522 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076509
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20100201
Package count4

External sources

Source: openFDA. Public-domain (CC0).