FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 0904-7539 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA213864
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20250522
Package count1

External sources

Source: openFDA. Public-domain (CC0).