Visitor Monitoring Drug History: IFEX/MESNEX KIT
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: IFEX/MESNEX KIT
FDA Application No: (NDA) 019763
Active Ingredient(s): IFOSFAMIDE; MESNA
Company: BRISTOL MYERS SQUIBB
 
Label History
 
View the label approved on April 7, 2003 for IFEXMESNEX KIT, (NDA) 019763


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
11/21/2001 014Package Change  
9/6/2001 013Manufacturing Change or Addition  
12/20/1996 009Manufacturing Change or Addition  
1/23/1996 008Control Supplement  
8/9/1995 007Labeling Revision  
6/15/1995 005Labeling Revision  
11/10/1992 004Labeling Revision  
11/10/1992 003Labeling Revision  
1/27/1992 002Control Supplement  
2/22/1990 001Control Supplement  
12/30/1988 000Approval Label 
 
There are no Therapeutic Equivalents
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