Visitor Monitoring Drug History: ACLOVATE
 
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: ACLOVATE
FDA Application No: (NDA) 018702
Active Ingredient(s): ALCLOMETASONE DIPROPIONATE
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on May 25, 2004 for ACLOVATE, (NDA) 018702


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
7/26/2002 008Manufacturing Change or Addition Letter
Label 
4/2/2003 007Labeling Revision Letter
Label 
6/22/1994 006Control Supplement  
4/26/1996 005Labeling Revision  
6/7/1994 004Manufacturing Change or Addition  
1/16/1991 003Manufacturing Change or Addition  
5/20/1986 002Control Supplement  
11/7/1983 001Labeling Revision  
12/14/1982 000Approval  
 
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