Visitor Monitoring Drug History: LOTRIMIN AF
 
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Label and Approval History

Drug Name: LOTRIMIN AF
FDA Application No: (NDA) 020890
Active Ingredient(s): CLOTRIMAZOLE
Company: SCHERING PLOUGH
 
Label History
 
View the label approved on April 25, 2003 for LOTRIMIN AF, (NDA) 020890


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/8/2001 005Control Supplement  
3/12/2001 004Control Supplement  
8/1/2001 002Labeling Revision Label 
10/26/1998 001Control Supplement  
10/27/1989 000Approval  
 
Therapeutic Equivalents
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