Drug History: CHILDREN'S MOTRIN

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 MOTRIN
FDA Application No:	(NDA) 020603
Active Ingredient(s):	IBUPROFEN
Company:	MCNEIL CONS

Label History

View the label approved on January 16, 2002 for CHILDREN'S MOTRIN, (NDA) 020603

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
2/27/2006	011	Labeling Revision	Letter
1/16/2002	005	Package Change	Letter Label
5/3/2001	004	Control Supplement
4/15/1999	003	Patient Population Altered	Review
9/13/1999	002	Labeling Revision	Letter Label Review
6/12/1998	001	Labeling Revision	Letter Label Review
6/10/1996	000	Approval

Therapeutic Equivalents