Drug History: NALFON

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:	NALFON
FDA Application No:	(NDA) 017604
Active Ingredient(s):	FENOPROFEN CALCIUM
Company:	PEDINOL

Label History

View the label approved on August 14, 2007 for NALFON, (NDA) 017604

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
8/7/2007	041	Labeling Revision	Letter Label
1/18/2006	040	Labeling Revision	Letter Label
8/21/2001	038	Control Supplement
11/24/1999	037	Control Supplement
9/30/1998	035	Manufacturing Change or Addition
4/2/1998	033	Package Change
12/22/1997	032	Control Supplement
1/22/1996	029	Control Supplement
4/25/1994	028	Manufacturing Change or Addition
3/29/1995	027	Labeling Revision
7/15/1987	024	Control Supplement
7/23/1987	023	Manufacturing Change or Addition
6/9/1986	022	Labeling Revision
12/11/1987	019	Manufacturing Change or Addition
3/31/1983	018	Labeling Revision
7/29/1983	017	Package Change
8/9/1983	016	Labeling Revision
7/14/1981	015	Labeling Revision
5/6/1980	014	Formulation Revision
8/9/1983	013	Labeling Revision
10/15/1980	012	Control Supplement
10/15/1980	009	General Efficacy (MarkIV)
10/24/1978	007	Expiration Date Change
4/1/1977	006	Control Supplement
9/23/1976	003	Expiration Date Change
3/16/1976	000	Approval

Therapeutic Equivalents