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) 012104
Active Ingredient(s): TRIAMCINOLONE ACETONIDE
Company: RANBAXY
 
Label History
 
Labels are not available on this site for KENALOG, (NDA) 012104
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/12/2001 028Manufacturing Change or Addition  
3/5/1997 027Manufacturing Change or Addition  
9/23/1992 026Manufacturing Change or Addition  
6/4/1987 025Control Supplement  
8/23/1985 024Package Change  
6/11/1985 023Manufacturing Change or Addition  
10/6/1983 022Manufacturing Change or Addition  
8/20/1982 021Practioner Draft Labeling  
7/21/1980 020Control Supplement  
10/2/1979 019Labeling Revision  
3/16/1979 018Control Supplement  
7/5/1978 017Labeling Revision  
10/11/1977 015Manufacturing Change or Addition  
10/11/1977 014Control Supplement  
6/23/1977 013Labeling Revision  
2/4/1977 012Manufacturing Change or Addition  
10/18/1976 011Labeling Revision  
10/11/1974 009Control Supplement  
10/11/1974 000Approval  
 
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