Drug History: PAMELOR

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	PAMELOR
FDA Application No:	(NDA) 018012
Active Ingredient(s):	NORTRIPTYLINE HYDROCHLORIDE
Company:	TYCO HLTHCARE

Label History

View the label approved on July 16, 2007 for PAMELOR, (NDA) 018012

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
7/13/2007	027	Labeling Revision	Letter Label
1/12/2005	026	Labeling Revision	Letter Label
7/31/2001	024	Labeling Revision	Label
12/23/1999	023	Control Supplement
3/29/1994	019	Control Supplement
3/26/1990	015	Manufacturing Change or Addition
4/13/1989	012	Control Supplement
8/25/1986	011	Control Supplement
6/11/1985	010	Labeling Revision
5/1/1984	008	Labeling Revision
7/7/1982	007	Manufacturing Change or Addition
3/25/1981	006	Package Change
1/31/1980	004	Formulation Revision
6/15/1979	003	Package Change
2/18/1982	002	Manufacturing Change or Addition
6/29/1978	001	General Efficacy (MarkIV)
8/1/1977	000	Approval	Other Important Information from FDA

Therapeutic Equivalents