Visitor Monitoring Drug History: KETOPROFEN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: KETOPROFEN
FDA Application No: (ANDA) 075270
Active Ingredient(s): KETOPROFEN
Company: ANDRX PHARMS
 
Label History
 
Labels are not available on this site for KETOPROFEN, (ANDA) 075270
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/24/2002 003Packager Addition  
9/20/2002 002Packager Addition  
2/4/2000 001Control Supplement  
3/24/1999 000Approval Letter 
 
Therapeutic Equivalents
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