Drug History: TRETINOIN

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:	TRETINOIN
FDA Application No:	(ANDA) 075265
Active Ingredient(s):	TRETINOIN
Company:	TRIAX PHARMS LLC

Label History

View the label approved on December 24, 1998 for TRETINOIN, (ANDA) 075265

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
10/24/2001	015	Manufacturing Revision
10/24/2001	014	Control Supplement
10/24/2001	013	Facility Addition
1/23/2001	012	Control Supplement
8/1/2000	009	Control Supplement
8/1/2000	008	Control Supplement
1/23/2001	007	Control Supplement
1/23/2001	006	Facility Addition
2/29/2000	005	Control Supplement
12/23/1999	003	Control Supplement
12/24/1998	000	Approval	Letter Label Review

Therapeutic Equivalents