Visitor Monitoring Drug History: VENTAVIS
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: VENTAVIS
FDA Application No: (NDA) 021779
Active Ingredient(s): ILOPROST
Company: ACTELION PHARM
 
Label History
 
View the label approved on December 15, 2005 for VENTAVIS, (NDA) 021779


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/8/2005 003Control Supplement Letter
Label 
8/24/2005 002Formulation Revision Letter
Label 
8/24/2005 001New or Modified Indication Letter
Label 
12/29/2004 000Approval Letter
Label
Review
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