| NDC Code | 0703-1995-01 |
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| Package Description | 1 VIAL in 1 CARTON (0703-1995-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
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| Product NDC | 0703-1995 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Epoprostenol Sodium |
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| Non-Proprietary Name | Epoprostenol Sodium |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20080423 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078396 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | EPOPROSTENOL SODIUM |
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| Strength | 1.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE] |
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