Visitor Monitoring Drug History: DAYPRO ALTA
 
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Label and Approval History

Drug Name: DAYPRO ALTA
FDA Application No: (NDA) 020776
Active Ingredient(s): OXAPROZIN POTASSIUM
Company: GD SEARLE
 
Label History
 
View the label approved on January 20, 2006 for DAYPRO ALTA, (NDA) 020776


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
7/5/2007 002Labeling Revision Letter 
1/18/2006 001Labeling Revision Letter
Label 
10/17/2002 000Approval Letter
Label
Review 
 
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