Drug History: NEGGRAM

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:	NEGGRAM
FDA Application No:	(NDA) 017430
Active Ingredient(s):	NALIDIXIC ACID
Company:	SANOFI AVENTIS US

Label History

View the label approved on August 6, 2007 for NEGGRAM, (NDA) 017430

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
8/3/2007	032	Labeling Revision	Letter Label
9/7/2004	030	Labeling Revision	Letter Label
9/7/2004	029	Labeling Revision	Letter Label
9/7/2004	028	Labeling Revision	Letter Label
11/23/1999	027	Labeling Revision	Review
11/23/1999	026	Labeling Revision	Review
10/31/1994	025	Control Supplement
8/3/1993	024	Control Supplement
6/24/1991	023	Control Supplement
5/13/1991	022	Control Supplement
7/30/1990	021	Package Change
7/13/1990	020	Control Supplement
2/7/1995	019	Labeling Revision
3/14/1988	018	Control Supplement
4/21/1986	017	Labeling Revision
8/21/1987	016	Labeling Revision
2/6/1984	015	Control Supplement
6/2/1983	013	Control Supplement
8/18/1981	012	Package Change
6/30/1980	011	Labeling Revision
2/23/1981	010	Labeling Revision
7/1/1977	009	Control Supplement
2/23/1977	007	Labeling Revision
9/23/1976	006	Formulation Revision
4/8/1976	004	Control Supplement
2/28/1975	003	Control Supplement
3/13/1975	002	Control Supplement
4/17/1973	000	Approval

There are no Therapeutic Equivalents