Drug History: ZYRTEC

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:	ZYRTEC
FDA Application No:	(NDA) 020346
Active Ingredient(s):	CETIRIZINE HYDROCHLORIDE
Company:	PFIZER

Label History

View the label approved on April 5, 2004 for ZYRTEC, (NDA) 020346

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
3/17/2004	011	Labeling Revision	Letter Label
7/19/2002	009	Control Supplement
10/21/2002	008	Patient Population Altered	Letter Label
2/25/2000	006	Labeling Revision
3/4/1999	005	Control Supplement
6/10/1998	004	Control Supplement
10/21/1997	003	Package Change
5/15/1998	002	New or Modified Indication	Letter Review
4/18/1997	001	Control Supplement
9/27/1996	000	Approval

Therapeutic Equivalents