| NDC Code | 68788-7230-1 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7230-1) |
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| Product NDC | 68788-7230 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Glipizide |
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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 | 20180806 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076159 |
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| Manufacturer | Preferred Pharmaceuticals Inc. |
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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 [EPC],Sulfonylurea Compounds [CS] |
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