FDA NDC Directory · JSON-LD · Markdown

Gemfibrozil

NDC 70518-1563 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA077836
Dosage form / routeTABLET · ORAL
Active ingredientsGEMFIBROZIL (600 mg/1)
Marketing started20181022
Package count2

External sources

Source: openFDA. Public-domain (CC0).