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FENOFIBRATE

NDC 73352-101 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefenofibrate
Labeler / ManufacturerTrifluent Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217732
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (40 mg/1)
Marketing started20250812
Package count1

External sources

Source: openFDA. Public-domain (CC0).