NDC Code | 70771-1869-8 |
Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (70771-1869-8) |
Product NDC | 70771-1869 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Sitagliptin And Metformin Hydrochloride |
Non-Proprietary Name | Sitagliptin And Metformin Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20240314 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA216743 |
Manufacturer | Zydus Lifesciences Limited |
Substance Name | METFORMIN HYDROCHLORIDE; SITAGLIPTIN |
Strength | 500; 50 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Biguanide [EPC], Biguanides [CS], Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA] |