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) 050512
Active Ingredient(s):	CEFADROXIL/CEFADROXIL HEMIHYDRATE
Company:	WARNER CHILCOTT

Label History

View the label approved on June 7, 2007 for DURICEF, (NDA) 050512

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	046	Labeling Revision	Letter Label
12/16/2003	045	Labeling Revision	Letter Label
5/3/2002	044	Labeling Revision	Letter Label
10/15/1996	043	Labeling Revision
1/20/1982	040	Labeling Revision
11/2/1981	039	Control Supplement
11/2/1981	038	Package Change
10/27/1981	037	Manufacturing Change or Addition
8/24/1981	036	Package Change
8/18/1981	035	Package Change
4/21/1981	033	Labeling Revision
4/3/1981	032	Labeling Revision
2/22/1980	031	Labeling Revision
1/31/1980	030	Labeling Revision
1/21/1980	029	Expiration Date Change
1/24/1980	028	Expiration Date Change
12/28/1979	027	Labeling Revision
10/25/1979	025	Labeling Revision
4/26/1979	024	Package Change
11/30/1979	023	Control Supplement
5/5/1980	022	Control Supplement
2/26/1979	021	Labeling Revision
8/14/1978	020	Expiration Date Change
7/21/1978	019	Package Change
7/7/1978	018	Manufacturing Change or Addition
5/8/1978	017	Labeling Revision
5/8/1978	016	Labeling Revision
9/12/1988	014	Control Supplement
5/18/1989	013	Labeling Revision
8/30/1991	011	New Dosage Regimen
11/18/1987	009	Manufacturing Change or Addition
9/12/1986	007	Labeling Revision
7/17/1982	005	Expiration Date Change
7/8/1983	003	Package Change
5/21/1982	002	Control Supplement
2/17/1978	000	Approval

There are no Therapeutic Equivalents