Visitor Monitoring Drug History: XALATAN
 
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: XALATAN
FDA Application No: (NDA) 020597
Active Ingredient(s): LATANOPROST
Company: PHARMACIA AND UPJOHN
 
Label History
 
View the label approved on August 26, 2002 for XALATAN, (NDA) 020597


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
7/14/2003 029Control Supplement Letter 
7/14/2003 028Labeling Revision Letter 
11/15/2002 026Manufacturing Change or Addition  
8/26/2002 025Package Change Letter
Label 
6/21/2002 024Package Change  
11/26/2001 023Control Supplement Label 
5/14/2001 022Package Change  
4/23/2001 020Control Supplement  
8/8/2001 019Labeling Revision Label 
8/25/2000 018Labeling Revision  
12/11/2000 017Control Supplement  
11/9/2000 016Package Change  
12/26/2000 014Labeling Revision  
6/2/2000 013Manufacturing Change or Addition  
10/8/1999 012Labeling Revision  
1/24/2000 011Manufacturing Change or Addition  
12/20/2002 010New or Modified Indication Letter
Label 
7/16/1999 008Labeling Revision  
3/22/1999 007Labeling Revision  
11/1/1998 006Package Change  
7/31/1998 005Manufacturing Change or Addition  
12/9/1998 002Control Supplement  
6/23/1998 001Labeling Revision  
6/5/1996 000Approval  
 
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