| NDC Code | 68382-655-06 |
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| Package Description | 30 TABLET in 1 BOTTLE (68382-655-06) |
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| Product NDC | 68382-655 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Glyburide And Metformin Hydrochloride |
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| Non-Proprietary Name | Glyburide And Metformin Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20160407 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206748 |
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| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
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| Substance Name | GLYBURIDE; METFORMIN HYDROCHLORIDE |
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| Strength | 5; 500 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |
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