Drug History: CHILDREN'S ADVIL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

Label and Approval History

Drug Name:	CHILDREN'S ADVIL
FDA Application No:	(NDA) 020589
Active Ingredient(s):	IBUPROFEN
Company:	WYETH CONS

Label History

View the label approved on March 23, 2005 for CHILDREN'S ADVIL, (NDA) 020589

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 Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
12/7/2005	019	Labeling Revision	Letter
3/18/2005	017	Labeling Revision	Letter Label
11/14/2002	015	Labeling Revision
8/2/2001	014	Control Supplement
8/2/2001	013	Formulation Revision	Label
9/17/2001	012	Control Supplement
7/14/2000	011	Package Change
3/30/2000	010	Control Supplement
8/25/2000	009	Labeling Revision
10/17/1999	008	Package Change
10/14/1998	006	Manufacturing Change or Addition
5/5/1998	004	Manufacturing Change or Addition
11/7/1997	001	Formulation Revision
6/27/1996	000	Approval

Therapeutic Equivalents