Visitor Monitoring Drug History: LOTRIMIN
 
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: LOTRIMIN
FDA Application No: (NDA) 017619
Active Ingredient(s): CLOTRIMAZOLE
Company: SCHERING PLOUGH
 
Label History
 
Labels are not available on this site for LOTRIMIN, (NDA) 017619
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/10/2002 035Control Supplement  
2/28/2001 034Control Supplement  
1/29/2001 033Control Supplement  
11/10/1998 032Package Change  
5/29/1998 031Control Supplement  
5/18/1998 030Control Supplement  
5/21/1992 027Manufacturing Change or Addition  
6/23/1992 026Control Supplement  
2/6/1990 025Control Supplement  
10/27/1989 022OTC Labeling  
10/29/1987 021Manufacturing Change or Addition  
6/18/1987 020Control Supplement  
9/12/1986 019Manufacturing Change or Addition  
5/20/1986 018Control Supplement  
4/23/1986 017Manufacturing Change or Addition  
5/20/1985 016Labeling Revision  
7/24/1985 015Package Change  
7/3/1984 014Labeling Revision  
7/3/1984 013Practioner Draft Labeling  
8/18/1981 012Control Supplement  
10/13/1981 011Control Supplement  
6/4/1981 010Control Supplement  
2/27/1980 009Distributor  
1/14/1980 008Labeling Revision  
5/18/1978 007Manufacturing Change or Addition  
1/16/1978 006Package Change  
9/15/1977 005Manufacturing Change or Addition  
8/9/1977 004Manufacturing Change or Addition  
4/13/1977 003Package Change  
9/16/1976 002Control Supplement  
5/22/1975 001Supplement  
3/18/1975 000Approval  
 
Therapeutic Equivalents
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