Visitor Monitoring Drug History: LOTRIMIN
 
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Label and Approval History

Drug Name: LOTRIMIN
FDA Application No: (NDA) 018813
Active Ingredient(s): CLOTRIMAZOLE
Company: SCHERING
 
Label History
 
Labels are not available on this site for LOTRIMIN, (NDA) 018813
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/10/2002 023Control Supplement  
3/6/2001 022Control Supplement  
9/7/2000 021Package Change  
5/14/1999 020Control Supplement  
5/18/1998 019Control Supplement  
7/2/1993 016Manufacturing Change or Addition  
2/12/1993 015Package Change  
6/23/1992 014Control Supplement  
10/25/1991 013Package Change  
3/7/1991 011Control Supplement  
4/6/1989 009Package Change  
10/27/1989 007OTC Labeling  
6/18/1987 006Control Supplement  
5/20/1986 005Control Supplement  
5/20/1985 004Labeling Revision  
4/16/1985 003Package Change  
8/6/1984 002Labeling Revision  
8/6/1984 001Control Supplement  
2/17/1984 000Approval  
 
Therapeutic Equivalents
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