Visitor Monitoring Drug Details: VENTAVIS
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: VENTAVIS
FDA Application No: (NDA) 021779
Active Ingredient(s): ILOPROST
Company: ACTELION PHARM
Original Approval or Tentative Approval Date: December 29, 2004
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
O Orphan drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
VENTAVIS ILOPROST20UGM/2ML (10UGM/ML)SOLUTION; INHALATION Prescription Yes None
VENTAVIS ILOPROST10UGM/ML (10UGM/ML)SOLUTION; INHALATION Prescription Yes None


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