| NDC Code | 66215-401-01 |
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| Package Description | 1 VIAL in 1 CARTON (66215-401-01) > 10 mL in 1 VIAL |
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| Product NDC | 66215-401 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Veletri |
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| Non-Proprietary Name | Epoprostenol Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20100422 |
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| Marketing Category Name | NDA |
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| Application Number | NDA022260 |
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| Manufacturer | Actelion Pharmaceuticals US, Inc. |
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| Substance Name | EPOPROSTENOL SODIUM |
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| Strength | 1500000 |
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| Strength Unit | ng/10mL |
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| Pharmacy Classes | Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE] |
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