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Fenofibrate

NDC 35561-346 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFENOFIBRATE
Labeler / ManufacturerBostal LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207805
Dosage form / routeCAPSULE · ORAL
Active ingredientsFENOFIBRATE (134 mg/1)
Marketing started20171117
Package count3

External sources

Source: openFDA. Public-domain (CC0).