FDA NDC Directory · JSON-LD · Markdown

Gemfibrozil

NDC 51655-143 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077836
Dosage form / routeTABLET · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started20170814
Package count4

External sources

Source: openFDA. Public-domain (CC0).