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) 012515
Active Ingredient(s): TRIAMCINOLONE DIACETATE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for KENACORT, (NDA) 012515
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/7/1993 021Labeling Revision  
6/30/1982 019Package Change  
8/21/1979 017Control Supplement  
7/17/1979 015Manufacturing Change or Addition  
3/21/1961 000Approval  
 
There are no Therapeutic Equivalents
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