Visitor Monitoring Drug History: IMDUR
 
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: IMDUR
FDA Application No: (NDA) 020225
Active Ingredient(s): ISOSORBIDE MONONITRATE
Company: SCHERING PLOUGH
 
Label History
 
Labels are not available on this site for IMDUR, (NDA) 020225
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/22/2003 008Labeling Revision Letter 
2/17/1999 007Labeling Revision  
12/18/1998 006Manufacturing Change or Addition  
1/27/1999 005Manufacturing Change or Addition  
12/17/1997 004Labeling Revision  
1/23/1998 003Manufacturing Change or Addition  
3/6/1996 002Labeling Revision  
3/30/1995 001Control Supplement  
8/12/1993 000Approval  
 
Therapeutic Equivalents
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