Visitor Monitoring Drug History: LIDEX
 
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: LIDEX
FDA Application No: (NDA) 016909
Active Ingredient(s): FLUOCINONIDE
Company: MEDICIS
 
Label History
 
Labels are not available on this site for LIDEX, (NDA) 016909
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/16/2005 049Control Supplement Letter 
9/26/2000 047Manufacturing Change or Addition  
7/22/1996 046Manufacturing Change or Addition  
11/16/1992 045Control Supplement  
4/24/1992 044Control Supplement  
3/12/1991 043Labeling Revision  
2/13/1990 042Control Supplement  
12/6/1989 041Control Supplement  
9/26/1989 040Formulation Revision  
2/10/1989 039Control Supplement  
8/29/1984 038Manufacturing Change or Addition  
5/16/1984 037Expiration Date Change  
9/7/1983 036Manufacturing Change or Addition  
4/21/1983 035Practioner Draft Labeling  
11/19/1982 033Manufacturing Change or Addition  
11/20/1981 032Manufacturing Change or Addition  
11/10/1981 031Control Supplement  
1/19/1981 030Package Change  
1/19/1981 029Package Change  
1/19/1981 028Package Change  
1/19/1981 027Package Change  
8/7/1980 026Package Change  
3/24/1981 025Control Supplement  
10/23/1979 024Manufacturing Change or Addition  
8/13/1979 023Manufacturing Change or Addition  
11/7/1978 022Expiration Date Change  
11/29/1978 021Control Supplement  
1/2/1979 020Labeling Revision  
11/30/1978 019Control Supplement  
7/5/1978 018Control Supplement  
4/11/1978 017Expiration Date Change  
12/14/1977 016Control Supplement  
6/4/1977 015Manufacturing Change or Addition  
1/11/1977 014Labeling Revision  
9/22/1971 000Approval  
 
©2019 Drugs That Causes a False Positive on a Drug Test