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) 017579
Active Ingredient(s):	TRETINOIN
Company:	JOHNSON AND JOHNSON

Label History

View the label approved on June 10, 2002 for RETINA, (NDA) 017579

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
3/20/2001	024	Package Change
6/10/2002	023	Labeling Revision	Letter Label
1/25/1999	022	Manufacturing Change or Addition
7/23/1998	021	Manufacturing Change or Addition
6/10/2002	020	Labeling Revision	Letter Label
6/10/2002	018	Labeling Revision	Letter Label
1/31/1992	016	Control Supplement
7/3/1990	015	Control Supplement
8/28/1990	014	Labeling Revision
8/28/1990	013	Labeling Revision
12/1/1989	012	Package Change
6/11/1985	010	Manufacturing Change or Addition
7/23/1986	009	Manufacturing Change or Addition
11/30/1982	008	Final Printed Labeling - MarkIV
7/29/1981	007	Control Supplement
4/28/1980	005	Distributor
10/23/1979	004	Control Supplement
12/1/1978	003	Labeling Revision
6/14/1977	002	Package Change
1/4/1977	001	Distributor
4/18/1975	000	Approval

Therapeutic Equivalents