Visitor Monitoring Drug History: IBUPROFEN
 
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: IBUPROFEN
FDA Application No: (ANDA) 070481
Active Ingredient(s): IBUPROFEN
Company: PAR PHARM
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 070481
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/8/2001 038Labeling  
6/8/2001 037Packaging Addition  
11/5/1998 036Chemistry  
1/14/1997 034Chemistry  
7/12/1996 033Chemistry  
7/15/1994 030Chemistry  
2/13/1995 029Chemistry in Effect  
1/11/1994 028Chemistry  
1/11/1994 027Chemistry  
1/11/1994 026Chemistry  
1/11/1994 025Chemistry  
11/29/1988 024SBA  
3/20/1989 023Chemistry  
3/20/1989 022Chemistry  
3/20/1989 021Chemistry  
3/20/1989 020Chemistry  
3/20/1989 019Chemistry  
10/25/1988 017Labeling  
12/14/1987 016Chemistry  
9/9/1987 013Chemistry  
5/18/1987 010Chemistry  
4/11/1986 006Chemistry  
1/29/1987 005Chemistry  
4/25/1986 002Chemistry  
10/18/1985 000Approval  
 
Therapeutic Equivalents
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