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) 019910
Active Ingredient(s):	ZIDOVUDINE
Company:	GLAXOSMITHKLINE

Label History

View the label approved on November 16, 2006 for RETROVIR, (NDA) 019910

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	032	Labeling Revision	Letter Label
5/10/2006	029	Labeling Revision	Letter Label
10/15/2003	027	Labeling Revision	Letter Label
12/18/2002	026	Labeling Revision	Letter Label
2/21/2002	025	Labeling Revision	Letter
10/5/2001	024	Labeling Revision	Label
2/1/2000	023	Control Supplement
2/26/1999	022	Manufacturing Change or Addition
3/30/2001	021	Labeling Revision	Letter Label Review
2/25/1998	020	Manufacturing Change or Addition
3/4/1998	019	Labeling Revision
10/4/1996	018	New or Modified Indication
7/20/1995	016	Labeling Revision
10/4/1996	015	New Dosage Regimen
2/6/1995	013	Control Supplement
10/7/1994	012	Labeling Revision
8/8/1994	011	New or Modified Indication
8/24/1993	010	Labeling Revision
10/19/1992	008	Expiration Date Change
8/8/1994	007	Labeling Revision
3/2/1990	004	Patient Population Altered
1/12/1990	003	New Dosage Regimen
5/2/1990	002	Patient Population Altered
5/25/1990	001	Labeling Revision
9/28/1989	000	Approval

Therapeutic Equivalents