Visitor Monitoring Drug History: MAXIDEX
 
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: MAXIDEX
FDA Application No: (NDA) 013422
Active Ingredient(s): DEXAMETHASONE
Company: ALCON
 
Label History
 
View the label approved on May 28, 2003 for MAXIDEX, (NDA) 013422


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
4/17/2003 035Labeling Revision Letter
Label 
12/11/2002 034Control Supplement  
12/4/2002 033Control Supplement  
2/4/2000 032Manufacturing Change or Addition  
8/17/1999 031Control Supplement  
4/7/1999 030Manufacturing Change or Addition  
2/5/1999 029Manufacturing Change or Addition  
3/11/1999 028Control Supplement  
8/4/1998 027Control Supplement  
10/17/1996 025Control Supplement  
9/26/1996 024Labeling Revision  
3/18/1996 023Control Supplement  
11/1/1995 022Control Supplement  
11/1/1995 021Control Supplement  
6/14/1995 020Package Change  
11/28/1989 019Control Supplement  
12/6/1989 018Manufacturing Change or Addition  
3/2/1988 017Manufacturing Change or Addition  
3/21/1984 016Control Supplement  
8/5/1983 015Manufacturing Change or Addition  
8/8/1984 014Control Supplement  
8/5/1981 013Control Supplement  
7/6/1979 011Control Supplement  
7/6/1979 010Labeling Revision  
5/31/1990 004Package Change  
6/20/1962 000Approval  
 
Therapeutic Equivalents
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