Visitor Monitoring Drug History: LIDEX
 
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: LIDEX
FDA Application No: (NDA) 017373
Active Ingredient(s): FLUOCINONIDE
Company: MEDICIS
 
Label History
 
Labels are not available on this site for LIDEX, (NDA) 017373
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/16/2005 038Control Supplement Letter 
9/26/2000 035Manufacturing Change or Addition  
7/22/1996 034Manufacturing Change or Addition  
11/16/1992 033Control Supplement  
4/24/1992 032Control Supplement  
3/12/1991 031Labeling Revision  
2/13/1990 030Control Supplement  
12/6/1989 029Control Supplement  
2/10/1989 028Control Supplement  
4/10/1985 027Labeling Revision  
8/29/1984 026Manufacturing Change or Addition  
9/7/1983 025Manufacturing Change or Addition  
12/6/1983 024Expiration Date Change  
4/21/1983 023Practioner Draft Labeling  
11/19/1982 021Manufacturing Change or Addition  
11/20/1981 020Manufacturing Change or Addition  
11/10/1981 019Control Supplement  
11/3/1981 018Control Supplement  
1/19/1981 017Package Change  
1/19/1981 016Package Change  
1/19/1981 015Package Change  
8/7/1980 014Package Change  
10/23/1979 013Manufacturing Change or Addition  
8/13/1979 012Manufacturing Change or Addition  
11/29/1978 011Control Supplement  
9/12/1978 010Labeling Revision  
10/13/1978 009Labeling Revision  
7/5/1978 008Control Supplement  
12/14/1977 007Control Supplement  
6/4/1977 006Manufacturing Change or Addition  
1/4/1977 005Labeling Revision  
1/23/1976 004Labeling Revision  
5/15/1973 000Approval  
 
Therapeutic Equivalents
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