Drug History: TENUATE

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
FDA Application No:	(NDA) 011722
Active Ingredient(s):	DIETHYLPROPION HYDROCHLORIDE
Company:	WATSON PHARMS

Label History

View the label approved on September 7, 2004 for TENUATE, (NDA) 011722

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	029	Labeling Revision	Letter Label
7/14/2000	028	Control Supplement
5/6/1999	027	Labeling Revision
2/2/1998	025	Labeling Revision
7/21/1988	024	Package Change
10/3/1986	022	Control Supplement
2/10/1984	021	Package Change
1/6/1984	020	Manufacturing Change or Addition
6/8/1983	019	Control Supplement
12/6/1982	018	Labeling Revision
6/17/1988	017	Labeling Revision
8/3/1983	016	Control Supplement
10/18/1982	015	Package Change
10/31/1979	014	Control Supplement
4/27/1978	013	Package Change
9/23/1976	011	Package Change
2/12/1976	010	Package Change
8/6/1959	000	Approval

Therapeutic Equivalents