Visitor Monitoring Drug History: DURICEF
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: DURICEF
FDA Application No: (NDA) 050528
Active Ingredient(s): CEFADROXIL/CEFADROXIL HEMIHYDRATE
Company: WARNER CHILCOTT
 
Label History
 
View the label approved on June 7, 2007 for DURICEF, (NDA) 050528


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 DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/5/2007 020Labeling Revision Letter
Label 
12/16/2003 019Labeling Revision Letter
Label 
5/3/2002 018Labeling Revision Letter
Label 
10/15/1996 017Labeling Revision  
2/28/1990 013Labeling Revision  
9/12/1988 010Control Supplement  
8/30/1991 009New Dosage Regimen  
11/18/1987 007Manufacturing Change or Addition  
9/12/1986 005Labeling Revision  
7/8/1983 003Package Change  
8/6/1980 000Approval  
 
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