| NDC Code | 12064-012-00 |
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| Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (12064-012-00) |
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| Product NDC | 12064-012 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Flolan |
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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 | 19951208 |
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| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
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| Application Number | NDA020444 |
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| Manufacturer | GlaxoSmithKline Manufacturing SpA |
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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 [Chemical/Ingredient],Vasodilation [PE] |
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