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) 086681
Active Ingredient(s):	ACETAMINOPHEN; CODEINE PHOSPHATE
Company:	PUREPAC PHARM

Label History

Labels are not available on this site for ACETAMINOPHEN AND CODEINE PHOSPHATE, (ANDA) 086681

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
11/2/2001	032	Control Supplement
4/18/2001	031	Control Supplement
4/7/1998	030	Chemistry
1/18/1996	029	Chemistry
9/29/1994	028	Labeling
7/19/1995	027	Chemistry
7/14/1994	027	Labeling
9/8/1993	026	Chemistry
2/26/1991	025	Labeling
11/15/1990	024	Labeling
6/29/1989	023	Labeling
7/3/1991	022	Chemistry
7/3/1991	021	Chemistry
1/10/1989	020	Chemistry
4/22/1987	019	Chemistry
11/14/1985	016	Chemistry
3/12/1985	015	Chemistry
10/18/1984	014	Chemistry
10/18/1984	013	Chemistry
10/18/1984	012	Chemistry
10/18/1984	011	Chemistry
12/6/1982	008	Chemistry
5/11/1979	000	Approval	Review