Visitor Monitoring Drug History: CARDURA
 
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Label and Approval History

Drug Name: CARDURA
FDA Application No: (NDA) 019668
Active Ingredient(s): DOXAZOSIN MESYLATE
Company: PFIZER
 
Label History
 
Labels are not available on this site for CARDURA, (NDA) 019668
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/28/2006 017Labeling Revision Letter 
9/13/2002 016Manufacturing Change or Addition  
1/23/2002 015Labeling Revision Letter 
10/10/2000 014Labeling Revision  
4/7/2000 013Package Change  
6/13/2003 012Labeling Revision Letter 
7/21/1998 011Control Supplement  
7/21/1998 010Manufacturing Change or Addition  
7/29/1997 009Labeling Revision  
9/13/1996 008Labeling Revision  
2/6/1995 007Labeling Revision  
7/18/1994 006Labeling Revision  
10/5/1993 005Package Change  
4/29/1993 004Labeling Revision  
11/2/1992 003Manufacturing Change or Addition  
7/6/1991 002Manufacturing Change or Addition  
5/14/1991 001Manufacturing Change or Addition  
11/2/1990 000Approval  
 
Therapeutic Equivalents
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