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Sitagliptin Phosphate

NDC 0781-5770 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA202387
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSITAGLIPTIN PHOSPHATE (100 mg/1)
Marketing started20260114
Package count3

External sources

Source: openFDA. Public-domain (CC0).