Visitor Monitoring Drug History: LEXIVA
 
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: LEXIVA
FDA Application No: (NDA) 021548
Active Ingredient(s): FOSAMPRENAVIR CALCIUM
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on October 15, 2007 for LEXIVA, (NDA) 021548


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
10/12/2007 013New Dosage Regimen Letter
Label 
11/14/2006 011Labeling Revision Letter
Label 
2/7/2007 010Labeling Revision Letter
Label 
8/7/2006 009Labeling Revision Letter
Label 
5/11/2006 008Labeling Revision Letter
Label 
3/10/2006 007Labeling Revision Letter
Label 
11/10/2005 005Labeling Revision Letter
Label 
6/13/2005 004Labeling Revision Letter
Label 
11/29/2004 002Labeling Revision Letter
Label 
10/20/2003 000Approval Letter
Label
Review 
 
There are no Therapeutic Equivalents
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