Visitor Monitoring Drug History: NASACORT AQ
 
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Label and Approval History

Drug Name: NASACORT AQ
FDA Application No: (NDA) 020468
Active Ingredient(s): TRIAMCINOLONE ACETONIDE
Company: SANOFI AVENTIS US
 
Label History
 
View the label approved on April 5, 2004 for NASACORT AQ, (NDA) 020468


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
3/8/2004 013Labeling Revision Letter
Label 
12/23/2003 012Labeling Revision Letter
Label 
12/17/2003 011Labeling Revision Letter
Label 
5/6/2002 008Package Change  
3/12/2002 007Manufacturing Change or Addition  
8/17/2000 005Control Supplement  
10/15/1996 003Control Supplement  
9/26/1997 002New or Modified Indication  
8/23/1996 001Control Supplement  
5/20/1996 000Approval  
 
Therapeutic Equivalents
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