FDA NDC Directory · JSON-LD · Markdown

Gemfibrozil

NDC 68382-553 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204189
Dosage form / routeTABLET · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started20190115
Package count7

External sources

Source: openFDA. Public-domain (CC0).