Visitor Monitoring Drug History: ADVIL
 
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: ADVIL
FDA Application No: (NDA) 018989
Active Ingredient(s): IBUPROFEN
Company: WYETH CONS
 
Label History
 
View the label approved on May 7, 2007 for ADVIL, (NDA) 018989


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/1/2007 067Labeling Revision Letter
Label 
4/4/2006 061Labeling Revision Letter 
4/17/2006 060Labeling Revision Letter 
7/16/2004 058Labeling Revision Letter 
9/26/2003 056Package Change Letter
Label 
4/24/2002 055Control Supplement Letter
Label 
8/2/2001 054Control Supplement  
9/7/2001 053Control Supplement Label 
11/15/2000 052Labeling Revision  
10/4/1999 051Manufacturing Change or Addition  
11/19/1999 050Control Supplement  
10/14/1998 049Manufacturing Change or Addition  
12/19/1996 048Formulation Revision  
12/3/1996 047Control Supplement  
4/3/1997 046Control Supplement  
8/1/1995 043Manufacturing Change or Addition  
4/4/1995 042Formulation Revision  
9/7/1994 041Manufacturing Change or Addition  
10/24/1994 040Package Change  
10/18/1993 039Control Supplement  
10/18/1993 038Manufacturing Change or Addition  
3/11/1994 037Labeling Revision  
3/11/1994 036Labeling Revision  
8/24/1990 034Package Change  
2/26/1993 033Control Supplement  
4/25/1991 031Control Supplement  
6/28/1989 030Manufacturing Change or Addition  
2/14/1989 029Control Supplement  
4/25/1991 028Package Change  
5/2/1988 027Package Change  
5/25/1988 026Manufacturing Change or Addition  
5/25/1988 025Manufacturing Change or Addition  
5/25/1988 023Control Supplement  
1/6/1987 022Manufacturing Change or Addition  
1/17/1987 021Manufacturing Change or Addition  
5/25/1988 018Package Change  
2/1/1988 017Package Change  
5/25/1988 016Package Change  
7/5/1986 015Labeling Revision  
12/24/1985 014Package Change  
5/30/1986 010Manufacturing Change or Addition  
10/5/1984 007Control Supplement  
10/19/1985 006Manufacturing Change or Addition  
9/17/1985 005Manufacturing Change or Addition  
12/18/1984 004Formulation Revision  
5/18/1984 000Approval  
 
Therapeutic Equivalents
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