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Gemfibrozil

NDC 71610-824 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078012
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started20110401
Package count4

External sources

Source: openFDA. Public-domain (CC0).