| NDC Code | 62756-059-40 |
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| Package Description | 1 VIAL in 1 CARTON (62756-059-40) / 10 mL in 1 VIAL |
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| Product NDC | 62756-059 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Epoprostenol |
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| Non-Proprietary Name | Epoprostenol |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210116 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210473 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | EPOPROSTENOL SODIUM |
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| Strength | .5 |
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| Strength Unit | mg/10mL |
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| Pharmacy Classes | Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE] |
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