Visitor Monitoring Drug History: TAVIST
 
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Label and Approval History

Drug Name: TAVIST
FDA Application No: (NDA) 018675
Active Ingredient(s): CLEMASTINE FUMARATE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for TAVIST, (NDA) 018675
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/11/2002 010Manufacturing Change or Addition  
6/14/1995 007Control Supplement  
8/30/1994 006Labeling Revision  
7/21/1994 004Control Supplement  
12/4/1987 002Control Supplement  
12/2/1986 001Control Supplement  
6/28/1985 000Approval  
 
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