Drug History: PROMETH PLAIN

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Label and Approval History

Drug Name:	PROMETH PLAIN
FDA Application No:	(ANDA) 085953
Active Ingredient(s):	PROMETHAZINE HYDROCHLORIDE
Company:	ACTAVIS MID ATLANTIC

Label History

Labels are not available on this site for PROMETH PLAIN, (ANDA) 085953

Approval History

Action Date	Supplement Number	Approval Type
10/3/2001	051	Control Supplement
10/3/2001	050	Package Change
12/13/2001	049	Package Change
11/20/2000	048	Package Change
6/17/1999	043	Chemistry
6/17/1999	042	Chemistry
8/4/1997	040	Chemistry
1/16/1997	039	Chemistry
7/5/1996	038	Chemistry
8/8/1996	037	Chemistry
8/8/1996	036	Chemistry
8/8/1996	034	Chemistry
8/8/1996	033	Chemistry
10/30/1997	032	Chemistry
10/30/1997	031	Chemistry
6/4/1993	027	Chemistry
9/28/1990	024	Chemistry
12/27/1990	023	Chemistry in Effect
5/1/1990	022	Labeling
5/1/1990	021	Labeling
11/21/1989	020	Labeling
5/16/1990	019	Chemistry
2/8/1989	017	Chemistry
2/8/1989	016	Chemistry
2/12/1986	014	Chemistry
4/5/1985	010	Chemistry
5/25/1983	008	Chemistry
8/21/1978	000	Approval