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) 050730
Active Ingredient(s):	AZITHROMYCIN
Company:	PFIZER

Label History

View the label approved on April 5, 2004 for ZITHROMAX, (NDA) 050730

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	012	Labeling Revision	Letter
3/24/2004	011	Labeling Revision	Letter Label
7/22/2002	010	Labeling Revision	Letter
12/4/2001	009	Manufacturing Change or Addition
10/16/2002	007	Labeling Revision	Letter
11/13/2000	005	New or Modified Indication	Letter Label Review
11/11/2000	004	Labeling Revision
1/20/2000	003	Package Change
11/19/1999	002	Manufacturing Change or Addition
8/12/1997	001	Control Supplement
6/12/1996	000	Approval

Therapeutic Equivalents