| NDC Code | 0591-0900-10 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-0900-10) |
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| Product NDC | 0591-0900 |
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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 | 20060401 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076467 |
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| Manufacturer | Watson Laboratories, Inc. |
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| Substance Name | GLIPIZIDE |
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| Strength | 2.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
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