Visitor Monitoring Drug History: BALZIVA-21
 
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Label and Approval History

Drug Name: BALZIVA-21
FDA Application No: (ANDA) 076198
Active Ingredient(s): ETHINYL ESTRADIOL; NORETHINDRONE
Company: BARR
 
Label History
 
Labels are not available on this site for BALZIVA21, (ANDA) 076198
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/22/2004 000Approval  
 
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