| NDC Code | 70710-2038-3 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-2038-3) |
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| Product NDC | 70710-2038 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sitagliptin And Metformin Hydrochloride |
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| Non-Proprietary Name | Sitagliptin And Metformin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20241031 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA216778 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | METFORMIN HYDROCHLORIDE; SITAGLIPTIN |
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| Strength | 1000; 100 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Biguanide [EPC], Biguanides [CS], Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA] |
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