Visitor Monitoring Drug History: PATADAY
 
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: PATADAY
FDA Application No: (NDA) 021545
Active Ingredient(s): OLOPATADINE HYDROCHLORIDE
Company: ALCON
 
Label History
 
View the label approved on June 12, 2007 for PATADAY, (NDA) 021545


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
6/8/2007 009Package Change Letter
Label 
6/8/2007 008Labeling Revision Letter
Label 
4/26/2007 006Labeling Revision Letter
Label 
10/4/2006 004Labeling Revision  
12/22/2004 000Approval Letter
Label
Review 
 
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