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Nateglinide

NDC 55111-328 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077461
Dosage form / routeTABLET · ORAL
Active ingredientsNATEGLINIDE (60 mg/1)
Marketing started20090909
Package count5

External sources

Source: openFDA. Public-domain (CC0).