| NDC Code | 68084-112-01 |
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| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-112-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-112-11) |
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| Product NDC | 68084-112 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Glipizide |
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| Proprietary Name Suffix | Er |
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| Non-Proprietary Name | Glipizide |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20080611 |
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| End Marketing Date | 20240531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076467 |
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| Manufacturer | American Health Packaging |
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| Substance Name | GLIPIZIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |
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