| NDC Code | 50436-0874-3 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (50436-0874-3) |
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| Product NDC | 50436-0874 |
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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 | Unit Dose Services |
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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 | Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS] |
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