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Fenofibrate

NDC 33342-339 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210248
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20241113
Package count4

External sources

Source: openFDA. Public-domain (CC0).