TYVASO - 66302-206-03 - (treprostinil)

Alphabetical Index


Drug Information of TYVASO

Product NDC: 66302-206
Proprietary Name: TYVASO
Non Proprietary Name: treprostinil
Active Ingredient(s): 1.74    mg/2.9mL & nbsp;   treprostinil
Administration Route(s): ORAL
Dosage Form(s): INHALANT
Coding System: National Drug Codes(NDC)

Labeler Information of TYVASO

Product NDC: 66302-206
Labeler Name: United Therapeutics Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022387
Marketing Category: NDA
Start Marketing Date: 20090814

Package Information of TYVASO

Package NDC: 66302-206-03
Package Description: 4 AMPULE in 1 BOX (66302-206-03) > 2.9 mL in 1 AMPULE

NDC Information of TYVASO

NDC Code 66302-206-03
Proprietary Name TYVASO
Package Description 4 AMPULE in 1 BOX (66302-206-03) > 2.9 mL in 1 AMPULE
Product NDC 66302-206
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name treprostinil
Dosage Form Name INHALANT
Route Name ORAL
Start Marketing Date 20090814
Marketing Category Name NDA
Labeler Name United Therapeutics Corp.
Substance Name TREPROSTINIL
Strength Number 1.74
Strength Unit mg/2.9mL
Pharmaceutical Classes Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE]

Complete Information of TYVASO


General Information