Visitor Monitoring Drug History: KETOPROFEN
 
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Label and Approval History

Drug Name: KETOPROFEN
FDA Application No: (ANDA) 073516
Active Ingredient(s): KETOPROFEN
Company: TEVA
 
Label History
 
Labels are not available on this site for KETOPROFEN, (ANDA) 073516
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/24/2001 016Control Supplement  
7/7/2000 015Facility Addition  
1/14/2000 014Facility Addition  
3/26/1999 013Chemistry  
7/14/1998 012Chemistry  
12/10/1997 011Chemistry  
5/13/1997 010Chemistry  
3/17/1998 009Labeling  
3/14/1997 008Chemistry  
3/14/1997 007Chemistry  
7/31/1995 005Chemistry  
2/16/1995 003Chemistry  
9/6/1994 002Chemistry  
7/15/1994 001Chemistry  
12/22/1992 000Approval  
 
Therapeutic Equivalents
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