Drug History: NASONEX

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:	NASONEX
FDA Application No:	(NDA) 020762
Active Ingredient(s):	MOMETASONE FUROATE MONOHYDRATE
Company:	SCHERING PLOUGH

Label History

View the label approved on December 30, 2004 for NASONEX, (NDA) 020762

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
12/15/2004	023	New or Modified Indication	Letter Label
12/18/2003	021	Labeling Revision	Letter Label
3/3/2003	014	Labeling Revision	Letter Review
9/13/2002	013	Control Supplement
1/11/2002	012	Manufacturing Change or Addition
7/17/2002	011	Patient Population Altered	Letter Label
2/22/2001	010	Control Supplement
12/1/2000	009	Labeling Revision
10/4/2000	008	Package Change
8/25/2004	007	Formulation Revision	Letter Label
4/16/1999	006	Control Supplement
12/2/1999	004	New or Modified Indication
11/2/1998	003	Package Change
6/11/1998	002	Manufacturing Change or Addition
11/18/1998	001	Efficacy Supplement with Clinical Data to Support	Letter Review
10/1/1997	000	Approval

There are no Therapeutic Equivalents