Drug History: GEODON

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:	GEODON
FDA Application No:	(NDA) 020825
Active Ingredient(s):	ZIPRASIDONE HYDROCHLORIDE
Company:	PFIZER

Label History

View the label approved on October 4, 2007 for GEODON, (NDA) 020825

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
10/2/2007	026	Labeling Revision	Letter Label
5/24/2007	024	Labeling Revision	Letter Label
3/2/2007	021	Labeling Revision	Letter Label
8/17/2005	017	Labeling Revision	Letter Label
8/17/2005	015	Labeling Revision	Letter Label
8/13/2004	012	Labeling Revision	Letter
8/19/2004	009	New or Modified Indication	Letter Label Other
12/23/2003	008	Labeling Revision	Letter
2/15/2002	006	Labeling Revision	Letter
6/25/2002	005	Manufacturing Change or Addition
1/22/2002	004	Expiration Date Change
5/25/2001	003	Manufacturing Change or Addition
5/25/2001	002	Package Change
6/7/2001	001	Package Change
2/5/2001	000	Approval	Letter Label Review Other Important Information from FDA

There are no Therapeutic Equivalents