FDA NDC Directory · JSON-LD · Markdown
NDC 0781-5802 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Sandoz Inc |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA202388 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | METFORMIN HYDROCHLORIDE (1000 mg/1) SITAGLIPTIN PHOSPHATE (50 mg/1) |
| Marketing started | 20251202 |
| Package count | 3 |
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