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) 020518
Active Ingredient(s):	ZIDOVUDINE
Company:	GLAXOSMITHKLINE

Label History

View the label approved on November 22, 2006 for RETROVIR, (NDA) 020518

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
11/20/2006	015	Labeling Revision	Letter Label
5/10/2006	013	Labeling Revision	Letter Label
10/15/2003	011	Labeling Revision	Letter Label
12/18/2002	010	Labeling Revision	Letter Label
2/21/2002	009	Labeling Revision	Letter
10/5/2001	008	Labeling Revision	Label
2/1/2000	007	Control Supplement
4/2/1999	006	Control Supplement
2/26/1999	005	Manufacturing Change or Addition
3/30/2001	004	Labeling Revision	Letter Label Review
6/12/1998	003	Manufacturing Change or Addition
3/4/1998	002	Labeling Revision
10/4/1996	001	Formulation Revision
12/19/1995	000	Approval

There are no Therapeutic Equivalents