Drug History: DAYPRO

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:	DAYPRO
FDA Application No:	(NDA) 018841
Active Ingredient(s):	OXAPROZIN
Company:	GD SEARLE

Label History

View the label approved on January 20, 2006 for DAYPRO, (NDA) 018841

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
6/21/2007	022	Labeling Revision	Letter
1/18/2006	021	Labeling Revision	Letter Label
4/10/2003	020	Labeling Revision	Letter Label
9/8/2000	018	Expiration Date Change
2/22/2000	017	Manufacturing Change or Addition
1/25/2002	016	Patient Population Altered	Letter Label
1/6/1998	015	Labeling Revision
1/6/1998	014	Labeling Revision
1/25/2002	012	Labeling Revision	Letter Label
5/8/1997	011	Control Supplement
6/11/1996	010	Manufacturing Change or Addition
1/6/1998	009	Labeling Revision
6/13/1996	008	Control Supplement
1/6/1998	007	Labeling Revision
9/10/1996	006	Control Supplement
4/6/1995	005	Labeling Revision
2/22/1995	004	Labeling Revision
11/3/1995	003	Control Supplement
12/27/1993	002	Labeling Revision
4/2/1993	001	Labeling Revision
10/29/1992	000	Approval

Therapeutic Equivalents