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) 017391
Active Ingredient(s): AZATHIOPRINE SODIUM
Company: PROMETHEUS LABS
 
Label History
 
View the label approved on July 29, 2005 for IMURAN, (NDA) 017391


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 013Labeling Revision Letter
Label 
9/26/1997 012Manufacturing Change or Addition  
12/19/2002 011Labeling Revision Letter 
11/9/1994 010Manufacturing Change or Addition  
9/2/1993 009Manufacturing Change or Addition  
3/23/1992 008Control Supplement  
8/30/1994 003Practioner Draft Labeling  
4/23/1982 002Labeling Revision  
9/20/1978 001Manufacturing Change or Addition  
7/19/1974 000Approval  
 
There are no Therapeutic Equivalents
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