Veletri - 66215-402-01 - (epoprostenol)

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Drug Information of Veletri

Product NDC: 66215-402
Proprietary Name: Veletri
Non Proprietary Name: epoprostenol
Active Ingredient(s): 1500000    ng/10mL & nbsp;   epoprostenol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Veletri

Product NDC: 66215-402
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: 66215-402-01
Package Description: 1 VIAL in 1 CARTON (66215-402-01) > 10 mL in 1 VIAL

NDC Information of Veletri

NDC Code 66215-402-01
Proprietary Name Veletri
Package Description 1 VIAL in 1 CARTON (66215-402-01) > 10 mL in 1 VIAL
Product NDC 66215-402
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name epoprostenol
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
Strength Number 1500000
Strength Unit ng/10mL
Pharmaceutical Classes Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Veletri


General Information