| NDC Code | 51655-337-26 |
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| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-337-26) |
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| Product NDC | 51655-337 |
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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 | 20200526 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204720 |
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| Manufacturer | Northwind Pharmaceuticals, LLC |
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| Substance Name | GLIPIZIDE |
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| Strength | 5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |
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