Visitor Monitoring Drug History: HYDROCODONE BITARTRATE AND IBUPROFEN
 
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Label and Approval History

Drug Name: HYDROCODONE BITARTRATE AND IBUPROFEN
FDA Application No: (ANDA) 076604
Active Ingredient(s): HYDROCODONE BITARTRATE; IBUPROFEN
Company: ANDRX PHARMS
 
Label History
 
Labels are not available on this site for HYDROCODONE BITARTRATE AND IBUPROFEN, (ANDA) 076604
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/31/2003 000Approval  
 
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