Drug History: ACETAMINOPHEN AND CODEINE PHOSPHATE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Label and Approval History

Drug Name:	ACETAMINOPHEN AND CODEINE PHOSPHATE
FDA Application No:	(ANDA) 085861
Active Ingredient(s):	ACETAMINOPHEN; CODEINE PHOSPHATE
Company:	ACTAVIS MID ATLANTIC

Label History

Labels are not available on this site for ACETAMINOPHEN AND CODEINE PHOSPHATE, (ANDA) 085861

Approval History

Action Date	Supplement Number	Approval Type
4/2/2001	047	Expiration Date Change
9/5/2000	046	Package Change
10/2/1997	044	Chemistry
8/24/1994	043	Labeling
9/22/1994	042	Chemistry
3/4/1993	041	Labeling in Effect
7/16/1993	040	Chemistry
7/16/1993	039	Chemistry
3/29/1993	038	Chemistry
4/3/1991	035	Chemistry
11/8/1990	033	Labeling
4/6/1992	030	Chemistry in Effect
11/8/1990	029	Labeling
5/18/1990	028	Labeling in Effect
5/18/1990	026	Labeling
3/16/1989	025	Labeling
9/14/1990	024	Chemistry
9/14/1990	023	Chemistry
2/8/1989	021	Chemistry
2/8/1989	020	Chemistry
5/11/1988	019	Labeling
5/18/1990	018	Labeling in Effect
12/19/1986	017	Chemistry
10/23/1986	016	Chemistry
5/5/1987	015	Chemistry
7/26/1985	014	Chemistry
5/21/1985	013	Chemistry
12/3/1982	012	Chemistry
6/20/1978	000	Approval