Drug History: CYTOVENE IV

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:	CYTOVENE IV
FDA Application No:	(NDA) 019661
Active Ingredient(s):	GANCICLOVIR SODIUM
Company:	ROCHE PALO

Label History

View the label approved on February 2, 2006 for CYTOVENE IV, (NDA) 019661

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
1/31/2006	030	Labeling Revision	Letter Label
10/25/2002	029	Control Supplement
9/23/2002	028	Manufacturing Change or Addition
3/21/2002	027	Control Supplement
5/11/2000	026	Control Supplement
3/30/2000	025	Expiration Date Change
12/1/2000	024	Labeling Revision
8/27/1999	023	Manufacturing Change or Addition
11/14/1997	022	Labeling Revision
5/23/1997	021	Manufacturing Change or Addition
5/29/1996	020	Labeling Revision
5/8/1996	019	Labeling Revision
8/8/1996	018	Control Supplement
7/20/1995	017	Control Supplement
4/28/1995	016	Package Change
1/20/1995	015	Labeling Revision
9/13/1994	014	Package Change
9/30/1994	013	Control Supplement
9/30/1992	012	Control Supplement
10/9/1992	011	Control Supplement
1/15/1993	010	Control Supplement
5/15/1992	008	New or Modified Indication
6/19/1992	007	Manufacturing Change or Addition
7/17/1992	006	Control Supplement
7/24/1990	004	Labeling Revision
2/9/1993	003	Control Supplement
1/11/1990	002	Labeling Revision
6/23/1989	000	Approval

Therapeutic Equivalents