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Remodulin
Remodulin - 66302-102-01 - (treprostinil)
Drug Information of Remodulin
| Product NDC: | 66302-102 |
| Proprietary Name: | Remodulin |
| Non Proprietary Name: | treprostinil |
| Active Ingredient(s): | 50 mg/20mL & nbsp; treprostinil |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Remodulin
| Product NDC: | 66302-102 |
| Labeler Name: | United Therapeutics Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021272 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020522 |
Package Information of Remodulin
| Package NDC: | 66302-102-01 |
| Package Description: | 1 VIAL in 1 BOX (66302-102-01) > 20 mL in 1 VIAL |
NDC Information of Remodulin
| NDC Code | 66302-102-01 |
| Proprietary Name | Remodulin |
| Package Description | 1 VIAL in 1 BOX (66302-102-01) > 20 mL in 1 VIAL |
| Product NDC | 66302-102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | treprostinil |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20020522 |
| Marketing Category Name | NDA |
| Labeler Name | United Therapeutics Corporation |
| Substance Name | TREPROSTINIL |
| Strength Number | 50 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes | Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE] |
