Drug History: PARNATE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	PARNATE
FDA Application No:	(NDA) 012342
Active Ingredient(s):	TRANYLCYPROMINE SULFATE
Company:	GLAXOSMITHKLINE

Label History

View the label approved on August 3, 2007 for PARNATE, (NDA) 012342

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	059	Labeling Revision	Letter Label
1/23/2006	057	Labeling Revision	Letter
1/23/2006	056	Labeling Revision	Letter
1/12/2005	055	Labeling Revision	Letter Label
10/23/2001	053	Labeling Revision
7/14/1997	052	Manufacturing Change or Addition
3/15/2001	051	Labeling Revision	Letter
3/15/2001	048	Labeling Revision	Letter
3/15/2001	046	Labeling Revision	Letter
3/15/2001	044	Labeling Revision	Letter
3/15/2001	040	Labeling Revision	Letter
3/15/2001	039	Labeling Revision	Letter
3/15/2001	037	Labeling Revision	Letter
2/24/1988	036	Labeling Revision
3/22/1984	031	General Efficacy (MarkIV)
3/22/1984	028	New or Modified Indication
4/6/1981	026	Labeling Revision
5/20/1980	022	Labeling Revision
6/20/1978	017	Labeling Revision
2/21/1961	000	Approval	Other Important Information from FDA

Therapeutic Equivalents