Drug History: ZYPREXA ZYDIS

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:	ZYPREXA ZYDIS
FDA Application No:	(NDA) 021086
Active Ingredient(s):	OLANZAPINE
Company:	LILLY

Label History

View the label approved on July 10, 2007 for ZYPREXA ZYDIS, (NDA) 021086

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
7/6/2007	023	Labeling Revision	Letter Label
7/6/2007	022	Labeling Revision	Letter Label
11/29/2006	020	Labeling Revision	Letter Label
2/23/2006	016	Labeling Revision	Letter Label
9/13/2005	015	Labeling Revision	Letter
2/16/2006	013	Labeling Revision
8/25/2006	011	Labeling Revision	Letter Label
2/16/2006	009	Labeling Revision
10/24/2001	003	Control Supplement
4/6/2000	000	Approval	Letter Label Review Patient Information Sheet

There are no Therapeutic Equivalents