| NDC Code | 70710-2036-6 |
|---|
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-2036-6) |
|---|
| Product NDC | 70710-2036 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Sitagliptin And Metformin Hydrochloride |
|---|
| Non-Proprietary Name | Sitagliptin And Metformin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20241031 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA216778 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| 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] |
|---|