| NDC Code | 52125-765-19 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (52125-765-19) |
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| Product NDC | 52125-765 |
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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 | 20131112 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077270 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
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| Strength | 2.5; 250 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
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