FDA NDC Directory · JSON-LD · Markdown

Gemfibrozil

NDC 76282-225 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerExelan Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077836
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started20061020
Package count3

External sources

Source: openFDA. Public-domain (CC0).