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) 072096
Active Ingredient(s): IBUPROFEN
Company: PERRIGO
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 072096
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/26/2002 042Control Supplement  
11/26/2002 041Control Supplement  
11/26/2002 040Control Supplement  
9/12/2001 037Labeling  
8/21/2001 036Control Supplement  
8/21/2001 035Package Change  
10/26/2000 034Labeling  
6/19/2001 032Facility Addition  
3/27/2000 031Control Supplement  
10/1/1999 030Control Supplement  
3/11/1999 029Labeling  
6/23/1999 025Chemistry  
6/23/1999 024Chemistry  
7/15/1996 023Labeling  
7/25/1997 022Chemistry  
7/25/1997 021Chemistry  
3/22/1996 020Chemistry  
7/22/1996 019Chemistry  
6/1/1995 017Chemistry  
7/15/1996 016Labeling  
4/6/1995 015Chemistry  
2/13/1995 014Chemistry  
7/11/1994 013Chemistry  
7/6/1994 012Chemistry in Effect  
1/11/1994 011Labeling  
1/11/1994 010Chemistry  
11/15/1993 009Chemistry  
7/3/1991 008Chemistry  
11/30/1992 007Chemistry  
11/30/1992 006Chemistry  
2/11/1993 005Chemistry  
3/28/1989 001Chemistry  
12/8/1987 000Approval  
 
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