Drug History: RETIN-A

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:	RETIN-A
FDA Application No:	(NDA) 016921
Active Ingredient(s):	TRETINOIN
Company:	JOHNSON AND JOHNSON

Label History

View the label approved on June 10, 2002 for RETINA, (NDA) 016921

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
6/10/2002	025	Labeling Revision	Letter Label
1/25/1999	024	Manufacturing Change or Addition
7/23/1998	023	Manufacturing Change or Addition
6/10/2002	022	Labeling Revision	Letter Label
6/10/2002	021	Labeling Revision	Letter Label
1/24/1992	020	Control Supplement
8/28/1990	019	Labeling Revision
7/22/1986	017	Manufacturing Change or Addition
6/6/1983	016	Manufacturing Change or Addition
7/28/1981	015	Control Supplement
12/13/1982	014	Practioner Draft Labeling
4/28/1980	013	Distributor
10/24/1979	012	Control Supplement
12/4/1978	011	Labeling Revision
1/4/1977	010	Distributor
9/20/1974	009	Control Supplement
10/20/1971	000	Approval

Therapeutic Equivalents