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Fenofibrate

NDC 68071-2369 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205118
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20160505
Package count1

External sources

Source: openFDA. Public-domain (CC0).