Visitor Monitoring Drug History: IBUPROFEN
 
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Label and Approval History

Drug Name: IBUPROFEN
FDA Application No: (ANDA) 073019
Active Ingredient(s): IBUPROFEN
Company: MCNEIL
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 073019
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/9/1997 010Chemistry  
10/7/1998 009Chemistry  
10/7/1998 008Chemistry  
10/7/1998 007Chemistry  
10/7/1998 006Labeling  
11/28/1997 005Chemistry  
10/7/1994 004Chemistry  
10/7/1994 003Chemistry  
11/28/1997 002Labeling  
11/28/1997 001Chemistry  
3/30/1994 000Approval  
 
Therapeutic Equivalents
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