Visitor Monitoring Drug History: IMITREX
 
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: IMITREX
FDA Application No: (NDA) 020132
Active Ingredient(s): SUMATRIPTAN SUCCINATE
Company: GLAXOSMITHKLINE
 
Label History
 
Labels are not available on this site for IMITREX, (NDA) 020132
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/17/2004 018Labeling Revision Letter 
6/30/2003 015Formulation Revision Review 
7/28/2003 015Labeling Revision Review 
7/28/2003 014Labeling Revision Letter
Review 
6/25/2001 012Labeling Revision  
6/25/2001 011Manufacturing Change or Addition  
2/9/2001 010Labeling Revision  
2/9/2001 008Labeling Revision  
2/9/2001 007Labeling Revision  
2/24/1998 006Labeling Revision  
12/16/1997 005Manufacturing Change or Addition  
2/13/1998 003New Dosage Regimen  
3/28/1996 001Manufacturing Change or Addition  
6/1/1995 000Approval Other Important Information from FDA 
 
There are no Therapeutic Equivalents
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