FDA NDC Directory · JSON-LD · Markdown

Sitagliptin and Metformin Hydrochloride

NDC 60505-3658 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA202426
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSITAGLIPTIN PHOSPHATE (50 mg/1)
METFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20260528
Package count2

External sources

Source: openFDA. Public-domain (CC0).