| NDC Code | 51655-087-52 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52) |
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| Product NDC | 51655-087 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Alfuzosin Hydrochloride |
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| Non-Proprietary Name | Alfuzosin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20221004 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079060 |
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| Manufacturer | Northwind Pharmaceuticals, LLC |
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| Substance Name | ALFUZOSIN HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC] |
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