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FLOLAN
FLOLAN - 0173-0519-00 - (epoprostenol sodium)
Drug Information of FLOLAN
| Product NDC: | 0173-0519 |
| Proprietary Name: | FLOLAN |
| Non Proprietary Name: | epoprostenol sodium |
| Active Ingredient(s): | 1.5 mg/1 & nbsp; epoprostenol sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLOLAN
| Product NDC: | 0173-0519 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020444 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19951208 |
Package Information of FLOLAN
| Package NDC: | 0173-0519-00 |
| Package Description: | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0519-00) |
NDC Information of FLOLAN
| NDC Code | 0173-0519-00 |
| Proprietary Name | FLOLAN |
| Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0519-00) |
| Product NDC | 0173-0519 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | epoprostenol sodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19951208 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | EPOPROSTENOL SODIUM |
| Strength Number | 1.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE] |
