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) 050693
Active Ingredient(s):	AZITHROMYCIN
Company:	PFIZER

Label History

View the label approved on April 5, 2004 for ZITHROMAX, (NDA) 050693

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	009	Labeling Revision	Letter
3/24/2004	008	Labeling Revision	Letter Label
7/22/2002	007	Labeling Revision	Letter
10/16/2002	005	Labeling Revision	Letter
11/13/2000	003	New or Modified Indication	Letter Label Review
11/11/2000	002	Labeling Revision
11/22/1999	001	Manufacturing Change or Addition
9/28/1994	000	Approval

There are no Therapeutic Equivalents