Drug History: CYCLOBENZAPRINE HYDROCHLORIDE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Label and Approval History

Drug Name:	CYCLOBENZAPRINE HYDROCHLORIDE
FDA Application No:	(ANDA) 071611
Active Ingredient(s):	CYCLOBENZAPRINE HYDROCHLORIDE
Company:	WATSON LABS

Label History

Labels are not available on this site for CYCLOBENZAPRINE HYDROCHLORIDE, (ANDA) 071611

Approval History

Action Date	Supplement Number	Approval Type
2/3/2006	040	Chemistry New Strength
2/3/2006	039	Chemistry New Strength
2/3/2006	038	Chemistry New Strength
4/25/2001	034	Control Supplement
12/29/2000	033	Control Supplement
12/23/1998	030	Chemistry
8/15/1996	029	Chemistry
8/15/1996	028	Chemistry
8/15/1996	027	Chemistry
8/15/1996	026	Chemistry
8/15/1996	025	Chemistry
8/15/1996	024	Chemistry
12/20/1993	023	Chemistry
6/29/1993	022	Labeling
3/12/1993	018	Labeling
3/12/1993	017	Chemistry
9/29/1992	016	Chemistry
9/29/1992	015	Chemistry
9/29/1992	014	Chemistry
2/23/1991	013	Chemistry
1/28/1991	012	Chemistry
5/31/1991	011	Chemistry
2/22/1990	010	Chemistry
6/29/1989	009	SBA
6/29/1990	009	Chemistry
2/23/1991	008	Chemistry
2/23/1991	007	Chemistry
2/23/1991	005	Chemistry
2/23/1991	004	Chemistry
2/23/1991	003	Chemistry
2/23/1991	002	Chemistry
4/20/1989	001	Chemistry
2/29/1988	000	Approval