Drug History: DURICEF

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:	DURICEF
FDA Application No:	(NDA) 050527
Active Ingredient(s):	CEFADROXIL/CEFADROXIL HEMIHYDRATE
Company:	WARNER CHILCOTT

Label History

View the label approved on June 7, 2007 for DURICEF, (NDA) 050527

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
6/5/2007	022	Labeling Revision	Letter Label
12/16/2003	021	Labeling Revision	Letter Label
5/3/2002	020	Labeling Revision	Letter Label
3/26/1999	019	Package Change
10/15/1996	017	Labeling Revision
5/21/1982	015	Control Supplement
1/20/1982	012	Labeling Revision
5/3/1989	011	Labeling Revision
9/12/1988	010	Formulation Revision
8/30/1991	009	New Dosage Regimen
10/27/1981	008	Manufacturing Change or Addition
3/5/1987	006	Control Supplement
8/7/1981	005	Labeling Revision
6/30/1981	004	Labeling Revision
3/31/1981	003	Labeling Revision
12/8/1980	002	Control Supplement
11/4/1980	001	Labeling Revision
9/12/1980	000	Approval

Therapeutic Equivalents