FDA NDC Directory · JSON-LD · Markdown

Gemfibrozil

NDC 75834-131 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNivagen Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203266
Dosage form / routeTABLET · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started20170215
Package count3

External sources

Source: openFDA. Public-domain (CC0).