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Fenofibrate

NDC 0378-4390 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefenofibrate
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204475
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (40 mg/1)
Marketing started20160623
Package count1

External sources

Source: openFDA. Public-domain (CC0).