Visitor Monitoring Drug History: IMURAN
 
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: IMURAN
FDA Application No: (NDA) 016324
Active Ingredient(s): AZATHIOPRINE
Company: PROMETHEUS LABS
 
Label History
 
View the label approved on July 29, 2005 for IMURAN, (NDA) 016324


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
7/26/2005 030Labeling Revision Letter
Label 
12/19/2002 026Labeling Revision Letter 
10/26/1992 022Control Supplement  
4/28/1992 021Manufacturing Change or Addition  
7/9/1992 020Manufacturing Change or Addition  
4/18/1988 017Control Supplement  
10/17/1989 016Package Change  
5/24/1988 014Package Change  
2/26/1987 013Control Supplement  
8/30/1994 011Labeling Revision  
4/13/1981 010General Efficacy (MarkIV)  
3/21/1980 008Control Supplement  
6/7/1978 007Control Supplement  
3/20/1968 000Approval  
 
Therapeutic Equivalents
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