Drug History: IFEX

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:	IFEX
FDA Application No:	(NDA) 019763
Active Ingredient(s):	IFOSFAMIDE
Company:	BRISTOL MYERS SQUIBB

Label History

View the label approved on April 7, 2003 for IFEX, (NDA) 019763

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
11/21/2001	014	Package Change
9/6/2001	013	Manufacturing Change or Addition
12/20/1996	009	Manufacturing Change or Addition
1/23/1996	008	Control Supplement
8/9/1995	007	Labeling Revision
6/15/1995	005	Labeling Revision
11/10/1992	004	Labeling Revision
11/10/1992	003	Labeling Revision
1/27/1992	002	Control Supplement
2/22/1990	001	Control Supplement
12/30/1988	000	Approval	Label

Therapeutic Equivalents