Visitor Monitoring Drug History: NAMENDA
 
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: NAMENDA
FDA Application No: (NDA) 021487
Active Ingredient(s): MEMANTINE HYDROCHLORIDE
Company: FOREST LABS
 
Label History
 
View the label approved on October 20, 2003 for NAMENDA, (NDA) 021487


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
10/4/2006 008Labeling Revision Letter 
4/19/2006 007Labeling Revision Letter 
5/17/2005 006Formulation Revision Letter 
5/2/2005 004Labeling Revision Letter 
9/22/2004 002Control Supplement Letter 
10/16/2003 000Approval Letter
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