| NDC Code | 59762-2332-3 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (59762-2332-3) |
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| Product NDC | 59762-2332 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20071114 |
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| End Marketing Date | 20160229 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077870 |
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| Manufacturer | Greenstone LLC |
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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 | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
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