FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 0904-7480 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA090856
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (145 mg/1)
Marketing started20250219
Package count2

External sources

Source: openFDA. Public-domain (CC0).