FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 33342-348 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210379
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20260121
Package count3

External sources

Source: openFDA. Public-domain (CC0).