Drug History: MAXIPIME

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:	MAXIPIME
FDA Application No:	(NDA) 050679
Active Ingredient(s):	CEFEPIME HYDROCHLORIDE (ARGININE FORMULATION)
Company:	BRISTOL MYERS SQUIBB

Label History

View the label approved on September 19, 2007 for MAXIPIME, (NDA) 050679

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
9/14/2007	028	Labeling Revision	Label
9/14/2007	024	Labeling Revision
6/9/2004	023	Supplement	Letter Label
3/17/2003	021	New Dosage Regimen	Letter Label
3/15/2002	020	Control Supplement
6/20/2001	019	Package Change
8/21/2002	018	Labeling Revision	Letter
4/2/2001	017	Package Change
5/10/2000	016	Manufacturing Change or Addition
6/26/2000	015	Labeling Revision
8/21/2002	014	Labeling Revision	Letter
9/20/2000	013	Labeling Revision
11/24/1998	012	Manufacturing Change or Addition
7/21/1998	011	Control Supplement
1/30/1998	010	Package Change
8/21/2002	009	Labeling Revision	Letter
1/30/1998	008	New or Modified Indication
1/27/1999	007	Labeling Revision	Letter Label Review
2/8/1999	005	Labeling Revision
10/20/1997	004	Manufacturing Change or Addition
12/23/1996	003	Control Supplement
5/16/1997	002	New or Modified Indication	Review
3/13/1996	001	Control Supplement
1/18/1996	000	Approval

Therapeutic Equivalents