Visitor Monitoring Drug History: KENACORT
 
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: KENACORT
FDA Application No: (NDA) 011283
Active Ingredient(s): TRIAMCINOLONE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for KENACORT, (NDA) 011283
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/7/1993 044Labeling Revision  
11/30/1987 043Manufacturing Change or Addition  
8/21/1979 040Control Supplement  
6/4/1979 038Labeling Revision  
7/17/1979 037Manufacturing Change or Addition  
7/17/1979 033Labeling Revision  
7/19/1968 003Supplement  
1/14/1958 000Approval  
 
Therapeutic Equivalents
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