Visitor Monitoring Drug History: KETOPROFEN
 
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Label and Approval History

Drug Name: KETOPROFEN
FDA Application No: (ANDA) 074879
Active Ingredient(s): KETOPROFEN
Company: ELAN PHARM
 
Label History
 
Labels are not available on this site for KETOPROFEN, (ANDA) 074879
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/18/2002 007Control Supplement  
9/25/2000 003Chemistry  
9/18/1998 002Chemistry  
9/8/1998 001Chemistry  
12/10/1997 000Approval Review 
 
Therapeutic Equivalents
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