Drug History: ZAROXOLYN

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:	ZAROXOLYN
FDA Application No:	(NDA) 017386
Active Ingredient(s):	METOLAZONE
Company:	UCB INC

Label History

View the label approved on June 16, 2003 for ZAROXOLYN, (NDA) 017386

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
8/19/2003	036	Labeling Revision	Letter
10/29/2002	034	Labeling Revision	Letter
4/15/2002	033	Control Supplement
8/10/2001	032	Labeling Revision	Label
10/18/2001	031	Control Supplement
8/13/1999	030	Labeling Revision
7/14/1997	029	Control Supplement
1/7/1997	027	Package Change
5/23/1995	026	Labeling Revision
5/4/1994	025	Control Supplement
1/13/1994	024	Labeling Revision
1/13/1993	023	Labeling Revision
10/10/1989	022	Labeling Revision
12/9/1988	021	Control Supplement
8/26/1987	020	Control Supplement
2/1/1988	019	Package Change
8/12/1985	018	Labeling Revision
2/7/1984	017	Control Supplement
2/7/1984	016	Package Change
9/30/1987	015	Practioner Draft Labeling
2/18/1983	014	Labeling Revision
7/15/1983	013	Control Supplement
7/15/1983	012	Control Supplement
12/2/1982	011	Formulation Revision
12/2/1982	010	Control Supplement
9/12/1989	009	Control Supplement
1/3/1980	008	Distributor
5/11/1977	006	Formulation Revision
4/25/1978	005	Labeling Revision
4/25/1978	004	Package Change
11/27/1973	000	Approval

Therapeutic Equivalents