Drug History: ZOSYN

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:	ZOSYN
FDA Application No:	(NDA) 050684
Active Ingredient(s):	PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Company:	WYETH PHARMS INC

Label History

View the label approved on July 27, 2006 for ZOSYN, (NDA) 050684

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
7/26/2006	046	Efficacy Supplement with Clinical Data to Support	Letter Label
9/30/2005	045	Formulation Revision	Letter Label Review
6/27/2005	044	Labeling Revision	Letter
3/15/2005	039	Labeling Revision	Letter
1/30/2004	038	Labeling Revision	Letter
5/1/2003	035	Labeling Revision	Letter Label
4/28/2003	033	New Dosage Regimen	Letter Label
12/4/2002	032	Package Change
10/10/2002	031	Control Supplement
3/15/2002	030	Control Supplement
3/15/2002	029	Expiration Date Change
3/14/2002	028	Control Supplement
2/26/2002	027	Control Supplement
12/19/2001	026	Control Supplement
8/20/2001	023	Package Change
2/1/2001	021	Control Supplement
11/22/2000	020	Manufacturing Change or Addition
11/21/2000	019	Control Supplement
8/1/2000	018	Control Supplement
8/1/2000	017	Control Supplement
8/1/2000	016	Package Change
3/27/2002	015	Labeling Revision	Letter
7/13/1998	013	Manufacturing Change or Addition
3/11/1999	012	Manufacturing Change or Addition
7/31/1997	011	Control Supplement
6/16/1997	010	Package Change
11/18/1996	009	Package Change
12/13/1996	008	Control Supplement
7/10/1995	007	Control Supplement
10/12/1994	005	Control Supplement
7/13/1994	004	Labeling Revision
8/24/1994	003	Package Change
7/13/1994	002	Labeling Revision
5/8/1996	001	New or Modified Indication
10/22/1993	000	Approval

There are no Therapeutic Equivalents