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Veletri
Veletri - 66215-401-01 - (epoprostenol sodium)
Drug Information of Veletri
| Product NDC: | 66215-401 |
| Proprietary Name: | Veletri |
| Non Proprietary Name: | epoprostenol sodium |
| Active Ingredient(s): | 1500000 ng/10mL & nbsp; epoprostenol sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Veletri
| Product NDC: | 66215-401 |
| Labeler Name: | Actelion Pharmaceuticals US, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022260 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100422 |
Package Information of Veletri
| Package NDC: | 66215-401-01 |
| Package Description: | 1 VIAL in 1 CARTON (66215-401-01) > 10 mL in 1 VIAL |
NDC Information of Veletri
| NDC Code | 66215-401-01 |
| Proprietary Name | Veletri |
| Package Description | 1 VIAL in 1 CARTON (66215-401-01) > 10 mL in 1 VIAL |
| Product NDC | 66215-401 |
| 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 | 20100422 |
| Marketing Category Name | NDA |
| Labeler Name | Actelion Pharmaceuticals US, Inc. |
| Substance Name | EPOPROSTENOL SODIUM |
| Strength Number | 1500000 |
| Strength Unit | ng/10mL |
| Pharmaceutical Classes | Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE] |
