Ventavis - 66215-302-30 - (iloprost)

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Drug Information of Ventavis

Product NDC: 66215-302
Proprietary Name: Ventavis
Non Proprietary Name: iloprost
Active Ingredient(s): .01    mg/mL & nbsp;   iloprost
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ventavis

Product NDC: 66215-302
Labeler Name: Actelion Pharmaceuticals US, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021779
Marketing Category: NDA
Start Marketing Date: 20050507

Package Information of Ventavis

Package NDC: 66215-302-30
Package Description: 30 AMPULE in 1 CARTON (66215-302-30) > 1 mL in 1 AMPULE (66215-302-00)

NDC Information of Ventavis

NDC Code 66215-302-30
Proprietary Name Ventavis
Package Description 30 AMPULE in 1 CARTON (66215-302-30) > 1 mL in 1 AMPULE (66215-302-00)
Product NDC 66215-302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name iloprost
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20050507
Marketing Category Name NDA
Labeler Name Actelion Pharmaceuticals US, Inc.
Substance Name ILOPROST
Strength Number .01
Strength Unit mg/mL
Pharmaceutical Classes Prostacycline [EPC],Prostaglandins I [Chemical/Ingredient]

Complete Information of Ventavis


General Information