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) 019655
Active Ingredient(s):	ZIDOVUDINE
Company:	GLAXOSMITHKLINE

Label History

View the label approved on November 16, 2006 for RETROVIR, (NDA) 019655

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	043	Labeling Revision	Letter Label
5/10/2006	041	Labeling Revision	Letter Label
10/15/2003	039	Labeling Revision	Letter Label
12/18/2002	038	Labeling Revision	Letter Label
2/21/2002	037	Labeling Revision	Letter
10/5/2001	036	Labeling Revision	Label
2/1/2000	035	Control Supplement
2/26/1999	034	Manufacturing Change or Addition
12/28/1998	033	Package Change
3/30/2001	032	Labeling Revision	Letter Label Review
11/4/1997	031	Manufacturing Change or Addition
3/4/1998	030	Labeling Revision
10/4/1996	029	New or Modified Indication
7/20/1995	027	Labeling Revision
10/4/1996	026	New Dosage Regimen
2/6/1995	025	Control Supplement
10/7/1994	024	Labeling Revision
8/8/1994	023	New or Modified Indication
8/24/1993	022	Labeling Revision
8/8/1994	020	Labeling Revision
5/2/1990	015	Labeling Revision
4/30/1990	014	Control Supplement
1/12/1990	013	New Dosage Regimen
8/24/1993	012	Labeling Revision
3/2/1990	011	Labeling Revision
3/13/1989	009	Package Change
3/6/1989	008	Manufacturing Change or Addition
10/13/1988	005	Formulation Revision
8/24/1993	003	Labeling Revision
4/21/1987	001	Manufacturing Change or Addition
3/19/1987	000	Approval

Therapeutic Equivalents