Drug History: TENUATE DOSPAN

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:	TENUATE DOSPAN
FDA Application No:	(NDA) 012546
Active Ingredient(s):	DIETHYLPROPION HYDROCHLORIDE
Company:	WATSON PHARMS

Label History

View the label approved on September 7, 2004 for TENUATE DOSPAN, (NDA) 012546

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
9/3/2004	032	Labeling Revision	Letter Label
4/16/2002	031	Formulation Revision
2/9/2000	030	Control Supplement
5/6/1999	029	Labeling Revision
2/2/1998	027	Labeling Revision
2/2/1998	025	Labeling Revision
7/21/1988	024	Package Change
10/3/1986	022	Control Supplement
8/22/1985	021	Package Change
12/23/1983	020	Manufacturing Change or Addition
6/8/1983	019	Control Supplement
12/6/1982	018	Labeling Revision
6/17/1988	017	Labeling Revision
10/18/1982	016	Package Change
11/6/1979	015	Control Supplement
4/27/1978	014	Package Change
9/27/1976	011	Package Change
6/24/1975	009	Control Supplement
11/17/1960	000	Approval

Therapeutic Equivalents