Drug History: VANTIN

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:	VANTIN
FDA Application No:	(NDA) 050675
Active Ingredient(s):	CEFPODOXIME PROXETIL
Company:	PHARMACIA AND UPJOHN

Label History

View the label approved on June 7, 2007 for VANTIN, (NDA) 050675

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
6/5/2007	017	Labeling Revision	Letter Label
6/2/2004	016	Labeling Revision	Letter Label
11/20/1998	015	New or Modified Indication	Letter Review
11/20/1998	014	New Dosage Regimen	Letter Review
3/19/1997	013	Labeling Revision
12/9/1996	012	Control Supplement
9/28/1995	011	Labeling Revision
3/14/1996	010	Labeling Revision
3/14/1996	009	New or Modified Indication
5/7/1996	008	New Dosage Regimen
7/6/1994	007	Labeling Revision
11/2/1993	006	Labeling Revision
10/20/1993	005	Labeling Revision
4/22/1993	004	Labeling Revision
6/16/1995	003	Comparative Efficacy Claim
4/8/1993	002	Labeling Revision
10/12/1993	001	Labeling Revision
8/7/1992	000	Approval

Therapeutic Equivalents