Drug History: ZEMPLAR

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:	ZEMPLAR
FDA Application No:	(NDA) 020819
Active Ingredient(s):	PARICALCITOL
Company:	ABBOTT

Label History

View the label approved on September 8, 2005 for ZEMPLAR, (NDA) 020819

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
9/2/2005	015	Labeling Revision	Letter Label
3/31/2004	014	Patient Population Altered	Letter Label
12/6/2002	012	Control Supplement
2/24/2003	011	Labeling Revision	Letter
1/25/2002	010	Manufacturing Change or Addition
1/8/2002	009	Expiration Date Change
2/24/2003	007	Labeling Revision	Letter
2/1/2000	006	Formulation Revision
10/18/1999	005	Control Supplement
9/13/2000	004	Labeling Revision
2/2/2000	003	Efficacy Supplement with Clinical Data to Support	Letter Label
4/17/1998	000	Approval	Letter Label Review Consumer Information Sheet

There are no Therapeutic Equivalents