Visitor Monitoring Drug History: KENALOG
 
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
FDA Application No: (NDA) 011600
Active Ingredient(s): TRIAMCINOLONE ACETONIDE
Company: APOTHECON
 
Label History
 
Labels are not available on this site for KENALOG, (NDA) 011600
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/18/1996 030Control Supplement  
7/9/1993 029Package Change  
4/4/1987 026Labeling Revision  
8/9/1984 025Manufacturing Change or Addition  
8/8/1984 024Manufacturing Change or Addition  
8/10/1983 023Package Change  
2/26/1981 022Control Supplement  
12/13/1982 021Practioner Draft Labeling  
7/5/1978 020Labeling Revision  
1/23/1980 019Control Supplement  
10/11/1977 018Manufacturing Change or Addition  
10/11/1977 017Control Supplement  
6/17/1977 016Labeling Revision  
2/4/1977 015Package Change  
7/15/1976 014Control Supplement  
6/11/1975 012Labeling Revision  
7/8/1974 010Supplement  
6/17/1977 000Approval  
 
Therapeutic Equivalents
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