Visitor Monitoring Drug History: LIDEX-E
 
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-E
FDA Application No: (NDA) 016908
Active Ingredient(s): FLUOCINONIDE
Company: MEDICIS
 
Label History
 
Labels are not available on this site for LIDEXE, (NDA) 016908
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/16/2005 058Control Supplement Letter 
9/26/2000 055Manufacturing Change or Addition  
1/27/1999 054Control Supplement  
7/22/1996 053Manufacturing Change or Addition  
3/1/1995 052Labeling Revision  
11/13/1992 051Control Supplement  
4/24/1992 050Control Supplement  
3/3/1995 049Labeling Revision  
2/13/1990 048Control Supplement  
12/6/1989 047Control Supplement  
2/10/1989 046Control Supplement  
8/29/1984 045Manufacturing Change or Addition  
9/7/1983 044Manufacturing Change or Addition  
4/8/1983 043Practioner Draft Labeling  
11/19/1982 041Manufacturing Change or Addition  
5/19/1982 040Expiration Date Change  
11/20/1981 039Manufacturing Change or Addition  
11/16/1981 038Manufacturing Change or Addition  
1/19/1981 037Package Change  
1/19/1981 036Package Change  
1/19/1981 035Package Change  
1/19/1981 034Package Change  
6/26/1981 033Package Change  
12/18/1979 030Control Supplement  
10/23/1979 029Manufacturing Change or Addition  
8/13/1979 028Manufacturing Change or Addition  
10/23/1981 027Labeling Revision  
11/29/1978 026Control Supplement  
11/1/1978 025Labeling Revision  
10/12/1978 024Labeling Revision  
9/12/1978 023Labeling Revision  
7/5/1978 022Control Supplement  
4/11/1978 021Control Supplement  
12/14/1977 020Control Supplement  
6/4/1977 019Control Supplement  
9/19/1977 018Formulation Revision  
1/4/1977 017Labeling Revision  
5/6/1976 016Control Supplement  
2/24/1976 015Supplement  
6/30/1971 000Approval  
 
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