Visitor Monitoring Drug History: ZERIT XR
 
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Label and Approval History

Drug Name: ZERIT XR
FDA Application No: (NDA) 021453
Active Ingredient(s): STAVUDINE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
View the label approved on January 21, 2005 for ZERIT XR, (NDA) 021453


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
1/19/2005 004Labeling Revision Letter
Label 
6/4/2004 003Labeling Revision Letter
Label 
12/31/2002 000Approval Letter
Label
Review 
 
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