Drug History: SINEQUAN

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:	SINEQUAN
FDA Application No:	(NDA) 016798
Active Ingredient(s):	DOXEPIN HYDROCHLORIDE
Company:	PFIZER

Label History

View the label approved on August 3, 2007 for SINEQUAN, (NDA) 016798

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
8/2/2007	054	Labeling Revision	Letter Label
2/18/2005	053	Labeling Revision	Letter
9/30/2003	050	Labeling Revision	Letter
4/10/2000	048	Labeling Revision
3/27/2000	047	Package Change
7/21/1994	044	Manufacturing Change or Addition
4/4/1990	043	Formulation Revision
10/27/1988	040	Control Supplement
10/27/1988	039	Control Supplement
9/1/1987	038	Package Change
10/28/1985	035	Package Change
9/13/1984	034	Labeling Revision
12/11/1984	033	Manufacturing Change or Addition
5/10/1984	032	Package Change
5/1/1984	031	Labeling Revision
9/26/1983	030	Package Change
9/26/1983	029	Package Change
7/22/1983	028	Control Supplement
2/12/1981	027	Package Change
8/12/1980	026	Formulation Revision
10/17/1979	025	Labeling Revision
7/7/1978	024	Control Supplement
7/12/1978	023	Package Change
6/6/1978	022	Formulation Revision
10/12/1977	021	Package Change
3/15/1978	020	Labeling Revision
3/15/1978	019	Manufacturing Change or Addition
10/28/1976	018	Package Change
3/11/1976	017	Control Supplement
6/4/1976	016	Control Supplement
4/7/1975	014	Control Supplement
3/31/1975	012	Control Supplement
6/13/1975	011	Distributor
9/23/1969	000	Approval	Other Important Information from FDA

Therapeutic Equivalents