Drug History: RETROVIR

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:	RETROVIR
FDA Application No:	(NDA) 019951
Active Ingredient(s):	ZIDOVUDINE
Company:	GLAXOSMITHKLINE

Label History

View the label approved on July 13, 2006 for RETROVIR, (NDA) 019951

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
11/15/2006	024	Labeling Revision	Letter
7/10/2006	023	Labeling Revision	Letter Label
8/19/2002	020	Manufacturing Change or Addition
7/25/2003	019	Labeling Revision	Letter Label
7/25/2003	018	Labeling Revision	Letter Label
2/21/2002	017	Labeling Revision	Letter
9/12/2001	016	Labeling Revision	Label
2/1/2000	015	Control Supplement
2/26/1999	014	Manufacturing Change or Addition
3/4/1998	012	Labeling Revision
8/18/1997	011	Manufacturing Change or Addition
2/12/1998	010	Labeling Revision
4/2/1996	009	Labeling Revision
3/22/1996	008	Labeling Revision
7/20/1995	007	Labeling Revision
2/6/1995	005	Control Supplement
10/7/1994	004	Labeling Revision
8/8/1994	003	New or Modified Indication
8/7/1992	001	Expiration Date Change
2/2/1990	000	Approval

There are no Therapeutic Equivalents