Visitor Monitoring Drug History: GLUCOPHAGE XR
 
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: GLUCOPHAGE XR
FDA Application No: (NDA) 021202
Active Ingredient(s): METFORMIN HYDROCHLORIDE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
View the label approved on November 6, 2006 for GLUCOPHAGE XR, (NDA) 021202


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
11/1/2006 015Labeling Revision Letter
Label 
3/19/2004 013Labeling Revision Letter 
3/19/2004 011Labeling Revision Letter 
4/11/2003 008Formulation Revision Letter
Label 
6/6/2002 006Expiration Date Change  
7/2/2002 005Manufacturing Change or Addition  
1/8/2002 004Manufacturing Change or Addition  
1/8/2002 003Labeling Revision Letter 
7/31/2001 002Manufacturing Change or Addition  
4/19/2001 001Labeling Revision Letter 
10/13/2000 000Approval Letter
Label
Review 
 
Therapeutic Equivalents
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