Remodulin - 66302-110-01 - (treprostinil)

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Drug Information of Remodulin

Product NDC: 66302-110
Proprietary Name: Remodulin
Non Proprietary Name: treprostinil
Active Ingredient(s): 200    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: 66302-110
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: 66302-110-01
Package Description: 1 VIAL in 1 BOX (66302-110-01) > 20 mL in 1 VIAL

NDC Information of Remodulin

NDC Code 66302-110-01
Proprietary Name Remodulin
Package Description 1 VIAL in 1 BOX (66302-110-01) > 20 mL in 1 VIAL
Product NDC 66302-110
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 200
Strength Unit mg/20mL
Pharmaceutical Classes Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Remodulin


General Information