Visitor Monitoring Drug History: RISEDRONATE SODIUM
 
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Label and Approval History

Drug Name: RISEDRONATE SODIUM
FDA Application No: (ANDA) 077132
Active Ingredient(s): RISEDRONATE SODIUM
Company: TEVA PHARMS
 
Label History
 
View the label approved on October 10, 2007 for RISEDRONATE SODIUM, (ANDA) 077132


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
8/11/2005 000Tentative Approval Letter
Label
Other Important Information from FDA 
10/5/2007 000Approval Letter
Label
Other Important Information from FDA 
 
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