Drug History: SANDIMMUNE

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:	SANDIMMUNE
FDA Application No:	(NDA) 050625
Active Ingredient(s):	CYCLOSPORINE
Company:	NOVARTIS

Label History

View the label approved on March 10, 2006 for SANDIMMUNE, (NDA) 050625

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
3/6/2006	044	Labeling Revision	Letter Label
7/19/2005	043	Labeling Revision	Letter Label
2/6/2004	040	Labeling Revision	Letter Label
2/6/2004	039	Labeling Revision	Letter Label
4/12/2002	034	Manufacturing Change or Addition
1/16/2002	033	Manufacturing Change or Addition
2/14/2003	032	Labeling Revision	Letter Label
2/14/2003	030	Labeling Revision	Letter Label
6/30/2000	029	Manufacturing Change or Addition
12/21/1999	028	Labeling Revision
10/4/2000	027	Labeling Revision
3/30/1998	025	Manufacturing Change or Addition
4/15/1996	024	Control Supplement
8/9/1996	023	Labeling Revision
11/21/1995	022	Labeling Revision
11/21/1995	021	Expiration Date Change
1/13/1995	020	Control Supplement
11/10/1994	019	Labeling Revision
3/7/1995	018	Manufacturing Change or Addition
5/9/1994	017	Control Supplement
5/9/1994	016	Control Supplement
5/17/1993	014	Package Change
11/2/1992	013	Package Change
3/19/1993	012	Control Supplement
11/23/1992	011	Control Supplement
2/21/1992	010	Control Supplement
6/10/1991	009	Labeling Revision
12/30/1992	007	Expiration Date Change
12/30/1992	006	Control Supplement
8/24/1990	003	Labeling Revision
11/21/1991	002	Package Change
3/2/1990	000	Approval

Therapeutic Equivalents