Drug History: MAXAQUIN

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:	MAXAQUIN
FDA Application No:	(NDA) 020013
Active Ingredient(s):	LOMEFLOXACIN HYDROCHLORIDE
Company:	PHARMACIA

Label History

View the label approved on March 18, 2005 for MAXAQUIN, (NDA) 020013

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
3/16/2005	015	Labeling Revision	Letter Label
3/6/2004	014	Labeling Revision	Letter Label
5/6/1999	013	Labeling Revision
5/6/1999	012	Labeling Revision
5/6/1999	011	Labeling Revision
9/11/1996	010	Labeling Revision
2/20/1997	009	Labeling Revision
10/24/2001	008	Labeling Revision	Label
10/9/1996	007	New or Modified Indication
9/27/1996	006	Labeling Revision
9/20/1993	003	Package Change
7/21/1993	002	Labeling Revision
2/21/1992	000	Approval

There are no Therapeutic Equivalents