Visitor Monitoring Drug History: KENALOG IN ORABASE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: KENALOG IN ORABASE
FDA Application No: (NDA) 012097
Active Ingredient(s): TRIAMCINOLONE ACETONIDE
Company: APOTHECON
 
Label History
 
View the label approved on September 3, 2002 for KENALOG IN ORABASE, (NDA) 012097


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/22/1996 027Control Supplement  
11/19/1993 026Package Change  
6/13/1990 025Manufacturing Change or Addition  
7/11/1988 024Control Supplement  
7/11/1988 023Expiration Date Change  
4/10/1987 021Manufacturing Change or Addition  
11/30/1987 020Manufacturing Change or Addition  
11/19/1986 019Package Change  
1/23/1986 018Formulation Revision  
8/11/1983 017Control Supplement  
9/3/2002 016Labeling Revision Letter
Label 
6/16/1982 015Control Supplement  
8/21/1979 014Control Supplement  
7/17/1979 012Manufacturing Change or Addition  
2/22/1978 009Final Printed Labeling - MarkIV  
5/9/1977 008Control Supplement  
5/9/1977 007Manufacturing Change or Addition  
2/8/1977 006Labeling Revision  
3/4/1960 000Approval  
 
Therapeutic Equivalents
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