| NDC Code | 16571-874-01 |
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| Package Description | 100 CAPSULE in 1 BOTTLE (16571-874-01) |
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| Product NDC | 16571-874 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phenoxybenzamine Hydrochloride |
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| Non-Proprietary Name | Phenoxybenzamine Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20260826 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204551 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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| Substance Name | PHENOXYBENZAMINE 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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