Drug History: CUTIVATE

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:	CUTIVATE
FDA Application No:	(NDA) 019958
Active Ingredient(s):	FLUTICASONE PROPIONATE
Company:	ALTANA

Label History

View the label approved on April 16, 2002 for CUTIVATE, (NDA) 019958

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
6/7/2000	014	Control Supplement
4/16/2002	013	Labeling Revision	Letter Label
1/21/1999	012	Manufacturing Change or Addition
6/17/1999	011	Labeling Revision	Letter Label
8/8/1997	010	Manufacturing Change or Addition
4/25/1997	009	Patient Population Altered
6/17/1999	008	Patient Population Altered	Letter Label Review
6/7/1995	007	Control Supplement
10/7/1994	006	Manufacturing Change or Addition
6/7/1994	005	Manufacturing Change or Addition
10/7/1994	004	Control Supplement
2/14/1991	002	Control Supplement
2/14/1991	001	Control Supplement
12/18/1990	000	Approval

Therapeutic Equivalents