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) 011601
Active Ingredient(s): TRIAMCINOLONE ACETONIDE
Company: APOTHECON
 
Label History
 
Labels are not available on this site for KENALOG, (NDA) 011601
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/15/1996 042Control Supplement  
6/4/1987 040Control Supplement  
4/15/1986 039Control Supplement  
8/8/1984 038Manufacturing Change or Addition  
3/18/1982 037Expiration Date Change  
12/13/1982 036Practioner Draft Labeling  
3/24/1980 035Labeling Revision  
4/17/1979 034Labeling Revision  
2/5/1979 033Control Supplement  
11/13/1978 032Formulation Revision  
7/5/1978 031Labeling Revision  
10/11/1977 029Manufacturing Change or Addition  
10/11/1977 028Control Supplement  
5/23/1977 027Labeling Revision  
5/27/1977 026Control Supplement  
1/31/1977 025Manufacturing Change or Addition  
7/8/1976 024Formulation Revision  
4/28/1976 023Formulation Revision  
6/12/1975 021Supplement  
5/17/1975 021Other Amendment  
3/6/1975 020Control Supplement  
3/6/1975 019Control Supplement  
9/13/1974 018Labeling Revision  
7/18/1974 017Supplement  
11/13/1978 000Approval  
 
Therapeutic Equivalents
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