FDA NDC Directory · JSON-LD · Markdown

GEMFIBROZIL

NDC 68071-2387 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameGemfibrozil
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214603
Dosage form / routeTABLET · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started20210120
Package count3

External sources

Source: openFDA. Public-domain (CC0).