| NDC Code | 0093-7456-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0093-7456-01) |
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| Product NDC | 0093-7456 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Glipizide And Metformin Hydrochloride |
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| Non-Proprietary Name | Glipizide And Metformin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20051028 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077270 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
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| Strength | 2.5; 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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