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) 071163
Active Ingredient(s): IBUPROFEN
Company: OHM
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 071163
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/16/2001 039Control Supplement  
8/31/2001 038Supplier Addition  
9/18/2000 037Manufacturing Revision  
7/8/1999 035Labeling  
11/18/1998 034Labeling  
10/6/1997 032Labeling  
8/5/1994 031Chemistry  
7/29/1993 030Labeling  
11/2/1992 029Labeling  
9/21/1992 028Chemistry  
9/21/1992 027Chemistry  
4/21/1993 026Labeling  
4/21/1993 025Chemistry  
4/2/1990 024Chemistry  
1/18/1990 023SBA  
2/26/1990 023Chemistry  
6/22/1989 021Labeling  
4/17/1990 020Chemistry  
5/18/1989 019Chemistry  
11/22/1988 018Chemistry  
11/22/1988 017Chemistry  
11/21/1991 016Labeling  
11/21/1991 015Chemistry  
11/21/1991 014Chemistry  
5/31/1989 013Chemistry  
5/31/1989 012Labeling  
6/3/1988 011Chemistry  
4/28/1988 010Chemistry  
4/28/1988 009Chemistry  
12/9/1986 005Chemistry  
2/10/1987 004Chemistry  
10/3/1986 002Chemistry  
10/3/1986 001Chemistry  
7/15/1986 000Approval  
 
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