Visitor Monitoring Drug History: NASACORT
 
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Label and Approval History

Drug Name: NASACORT
FDA Application No: (NDA) 019798
Active Ingredient(s): TRIAMCINOLONE ACETONIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for NASACORT, (NDA) 019798
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/17/2000 011Control Supplement  
6/12/1997 009Package Change  
7/2/1996 007Package Change  
5/20/1996 006New or Modified Indication  
11/21/1996 005Manufacturing Change or Addition  
5/6/1994 002Labeling Revision  
11/30/1992 001Manufacturing Change or Addition  
7/11/1991 000Approval  
 
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