Drug History: INFUMORPH

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:	INFUMORPH
FDA Application No:	(NDA) 018565
Active Ingredient(s):	MORPHINE SULFATE
Company:	BAXTER HLTHCARE

Label History

View the label approved on June 8, 2005 for INFUMORPH, (NDA) 018565

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
6/6/2005	014	Labeling Revision	Letter Label
5/27/2004	012	Labeling Revision	Letter
6/26/2003	010	Labeling Revision	Letter
12/7/2001	009	Labeling Revision
6/14/1999	008	Control Supplement
4/17/1998	007	Control Supplement
2/12/1997	006	Control Supplement
4/28/1994	005	Labeling Revision
5/3/1989	004	Labeling Revision
7/19/1991	003	Labeling Revision
7/19/1991	002	Control Supplement
8/22/1985	001	Labeling Revision
9/18/1984	000	Approval

There are no Therapeutic Equivalents