Drug History: DAUNOXOME

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:	DAUNOXOME
FDA Application No:	(NDA) 050704
Active Ingredient(s):	DAUNORUBICIN CITRATE
Company:	GILEAD

Label History

View the label approved on April 7, 2003 for DAUNOXOME, (NDA) 050704

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
2/10/2002	012	Manufacturing Change or Addition
5/23/2000	011	Manufacturing Change or Addition
10/28/1999	010	Manufacturing Change or Addition
3/28/2000	009	Control Supplement
2/21/2002	008	Labeling Revision	Letter
3/23/1999	007	Control Supplement
2/26/1998	006	Control Supplement
2/26/1998	005	Expiration Date Change
2/24/1997	004	Control Supplement
3/11/1997	003	Expiration Date Change
10/11/1996	002	Control Supplement
8/27/1996	001	Control Supplement
4/8/1996	000	Approval	Label

There are no Therapeutic Equivalents