Visitor Monitoring Drug History: DEPODUR
 
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Label and Approval History

Drug Name: DEPODUR
FDA Application No: (NDA) 021671
Active Ingredient(s): MORPHINE SULFATE
Company: PACIRA PHARMS INC
 
Label History
 
View the label approved on February 23, 2007 for DEPODUR, (NDA) 021671


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
2/15/2007 015Labeling Revision Letter
Label 
1/17/2007 014Labeling Revision Letter
Label 
5/22/2006 004Labeling Revision Letter
Label 
8/11/2004 002Labeling Revision Letter 
5/18/2004 000Approval Letter
Label
Review 
 
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