Visitor Monitoring Drug History: IBUPROFEN
 
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Label and Approval History

Drug Name: IBUPROFEN
FDA Application No: (ANDA) 071935
Active Ingredient(s): IBUPROFEN
Company: INTERPHARM
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 071935
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/25/2001 017Manufacturing Revision  
4/12/2000 016Manufacturing Revision  
4/12/2000 015Control Supplement  
8/30/1999 014Labeling  
4/12/2000 013Facility Addition  
9/24/1999 011Chemistry  
2/11/1999 010Chemistry  
7/24/1997 009Chemistry  
1/20/1998 008Chemistry  
1/30/1992 007Labeling  
6/30/1988 004Chemistry  
3/28/1988 003Labeling  
2/17/1988 002Chemistry  
2/17/1988 001Chemistry  
10/13/1987 000Approval  
 
Therapeutic Equivalents
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