| NDC Code | 57237-114-05 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-05) |
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| Product NDC | 57237-114 |
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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 | 20120830 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079060 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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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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