NDC Code | 0173-0519-00 |
Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0519-00) |
Product NDC | 0173-0519 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Flolan |
Non-Proprietary Name | Epoprostenol Sodium |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 19951208 |
Marketing Category Name | NDA |
Application Number | NDA020444 |
Manufacturer | GlaxoSmithKline LLC |
Substance Name | EPOPROSTENOL SODIUM |
Strength | 1.5 |
Strength Unit | mg/1 |
Pharmacy Classes | Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE] |