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Nateglinide

NDC 72241-003 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerModavar Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206432
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsNATEGLINIDE (120 mg/1)
Marketing started20210819
Package count2

External sources

Source: openFDA. Public-domain (CC0).