Visitor Monitoring Drug History: CLEMASTINE FUMARATE
 
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Label and Approval History

Drug Name: CLEMASTINE FUMARATE
FDA Application No: (ANDA) 074863
Active Ingredient(s): CLEMASTINE FUMARATE
Company: MORTON GROVE
 
Label History
 
Labels are not available on this site for CLEMASTINE FUMARATE, (ANDA) 074863
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/18/2002 001Control Supplement  
3/13/1998 000Approval  
 
Therapeutic Equivalents
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