Visitor Monitoring Drug History: LOTRIMIN
 
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Label and Approval History

Drug Name: LOTRIMIN
FDA Application No: (NDA) 017613
Active Ingredient(s): CLOTRIMAZOLE
Company: SCHERING PLOUGH
 
Label History
 
Labels are not available on this site for LOTRIMIN, (NDA) 017613
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/28/2001 027Control Supplement  
3/8/2001 026Control Supplement  
9/7/2000 025Package Change  
5/28/1998 024Control Supplement  
5/18/1998 023Control Supplement  
6/23/1992 020Control Supplement  
10/25/1991 019Package Change  
4/6/1989 017Package Change  
10/27/1989 015OTC Labeling  
6/18/1987 014Control Supplement  
5/20/1986 013Control Supplement  
5/20/1985 012Labeling Revision  
7/3/1984 011Labeling Revision  
8/6/1984 010Control Supplement  
7/3/1984 009Practioner Draft Labeling  
8/5/1981 008Control Supplement  
4/9/1980 007Package Change  
5/18/1978 006Manufacturing Change or Addition  
9/13/1977 005Manufacturing Change or Addition  
8/9/1977 004Manufacturing Change or Addition  
4/13/1977 003Labeling Revision  
6/29/1976 002Labeling Revision  
4/22/1975 001Labeling Revision  
2/3/1975 000Approval  
 
Therapeutic Equivalents
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