Visitor Monitoring Drug History: KENALOG-10
 
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: KENALOG-10
FDA Application No: (NDA) 012041
Active Ingredient(s): TRIAMCINOLONE ACETONIDE
Company: APOTHECON
 
Label History
 
View the label approved on November 22, 2006 for KENALOG10, (NDA) 012041


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
6/15/2001 034Manufacturing Change or Addition  
11/20/2006 033Labeling Revision Letter
Label 
2/3/1998 032Control Supplement  
5/22/1996 031Control Supplement  
1/10/1995 030Control Supplement  
8/30/1993 029Package Change  
8/30/1993 028Package Change  
10/6/1993 027Labeling Revision  
9/25/1991 026Control Supplement  
7/19/1991 025Package Change  
11/19/1986 024Manufacturing Change or Addition  
11/30/1987 023Manufacturing Change or Addition  
12/3/1985 022Manufacturing Change or Addition  
4/1/1981 021Control Supplement  
8/21/1979 019Control Supplement  
5/20/1980 018Control Supplement  
7/17/1979 017Manufacturing Change or Addition  
9/19/1977 016Control Supplement  
1/12/1982 014Labeling Revision  
12/28/1978 013Labeling Revision  
1/4/1960 000Approval  
 
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