Drug History: DESFERAL

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:	DESFERAL
FDA Application No:	(NDA) 016267
Active Ingredient(s):	DEFEROXAMINE MESYLATE
Company:	NOVARTIS

Label History

View the label approved on January 24, 2007 for DESFERAL, (NDA) 016267

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
1/19/2007	044	Labeling Revision	Letter Label
1/15/2002	040	Manufacturing Change or Addition
2/14/2002	039	Labeling Revision	Letter
7/5/2001	038	Control Supplement
4/24/2002	037	Control Supplement
1/5/2001	036	Control Supplement
4/28/2000	035	Manufacturing Change or Addition
4/9/2001	034	Labeling Revision	Letter
5/25/2000	033	Package Change
10/23/1998	032	Manufacturing Change or Addition
12/22/1998	031	Manufacturing Change or Addition
12/22/1998	030	Package Change
12/22/1998	029	Manufacturing Change or Addition
4/2/1997	028	Labeling Revision
6/19/1995	027	Labeling Revision
8/31/1994	026	Labeling Revision
1/30/1998	025	Control Supplement
1/30/1998	024	Manufacturing Change or Addition
2/12/1990	022	Package Change
9/8/1987	021	Labeling Revision
2/13/1987	020	Labeling Revision
9/27/1985	019	Control Supplement
1/8/1986	018	Control Supplement
1/4/1984	017	Package Change
4/6/1984	016	Control Supplement
4/17/1986	015	Practioner Draft Labeling
9/2/1980	014	Manufacturing Change or Addition
7/8/1980	013	Package Change
6/4/1979	012	Labeling Revision
6/4/1979	011	General Efficacy (MarkIV)
4/6/1978	010	Manufacturing Change or Addition
1/25/1978	009	Control Supplement
3/4/1977	008	Other Amendment
1/20/1976	007	Labeling Revision
4/1/1968	000	Approval

Therapeutic Equivalents