FDA NDC Directory · JSON-LD · Markdown

Gemfibrozil

NDC 62135-160 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074270
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started19930927
Package count2

External sources

Source: openFDA. Public-domain (CC0).