| NDC Code | 67209-066-02 |
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| Package Description | 48 BOTTLE in 1 BOX (67209-066-02) > 100 CAPSULE in 1 BOTTLE |
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| Product NDC | 67209-066 |
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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 | 20150811 |
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| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
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| Application Number | NDA008708 |
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| Manufacturer | WellSpring Pharma Services 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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