Visitor Monitoring Drug History: ACTRON
 
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Label and Approval History

Drug Name: ACTRON
FDA Application No: (NDA) 020499
Active Ingredient(s): KETOPROFEN
Company: BAYER
 
Label History
 
Labels are not available on this site for ACTRON, (NDA) 020499
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/17/1996 002Manufacturing Change or Addition  
11/3/1995 001Labeling Revision  
10/6/1995 000Approval Review 
 
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