Visitor Monitoring Drug History: ZADITOR
 
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: ZADITOR
FDA Application No: (NDA) 021066
Active Ingredient(s): KETOTIFEN FUMARATE
Company: NOVARTIS
 
Label History
 
View the label approved on October 23, 2006 for ZADITOR, (NDA) 021066


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
10/19/2006 011OTC Labeling Letter
Label 
10/4/2002 005Control Supplement  
7/20/2001 004Labeling Revision Label 
12/26/2000 003Manufacturing Change or Addition  
7/24/2000 002Package Change  
3/8/2000 001Labeling Revision  
7/2/1999 000Approval Letter
Label
Review
Patient Information Sheet 
 
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