FDA NDC Directory · JSON-LD · Markdown

Repaglinide

NDC 57237-159 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203820
Dosage form / routeTABLET · ORAL
Active ingredientsREPAGLINIDE (2 mg/1)
Marketing started20140122
Package count2

External sources

Source: openFDA. Public-domain (CC0).