FDA NDC Directory · JSON-LD · Markdown

NATEGLINIDE

NDC 16571-758 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205544
Dosage form / routeTABLET · ORAL
Active ingredientsNATEGLINIDE (60 mg/1)
Marketing started20201216
Package count3

External sources

Source: openFDA. Public-domain (CC0).