Drug History: ZITHROMAX

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:	ZITHROMAX
FDA Application No:	(NDA) 050733
Active Ingredient(s):	AZITHROMYCIN
Company:	PFIZER

Label History

View the label approved on May 2, 2003 for ZITHROMAX, (NDA) 050733

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
1/15/2004	013	Labeling Revision	Letter
1/15/2004	012	Labeling Revision	Letter
7/22/2002	010	Labeling Revision	Letter
3/13/2002	009	Package Change	Letter
12/10/2001	008	Manufacturing Change or Addition
6/12/2003	007	Labeling Revision	Letter
10/16/2002	006	Labeling Revision	Letter
2/28/2001	005	Labeling Revision	Label
11/11/2000	004	Labeling Revision
11/22/1999	003	Manufacturing Change or Addition
10/19/1999	002	Manufacturing Change or Addition
7/20/1999	001	Labeling Revision
1/30/1997	000	Approval	Review

Therapeutic Equivalents