Visitor Monitoring Drug History: MEFOXIN
 
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: MEFOXIN
FDA Application No: (NDA) 050517
Active Ingredient(s): CEFOXITIN SODIUM
Company: MERCK
 
Label History
 
View the label approved on September 19, 2007 for MEFOXIN, (NDA) 050517


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
9/17/2007 047Labeling Revision Letter
Label 
6/2/2004 046Labeling Revision Letter
Label 
6/28/2004 045Labeling Revision Letter 
6/6/2002 044Manufacturing Change or Addition  
5/7/2002 043Control Supplement  
6/28/2004 042Labeling Revision Letter 
10/19/2001 041Control Supplement  
10/12/1999 040Control Supplement  
4/24/1997 039Labeling Revision Review 
2/14/2000 038Labeling Revision Review 
11/30/1994 036Control Supplement  
5/20/1996 035Labeling Revision  
10/27/1994 033Labeling Revision  
5/20/1996 032Labeling Revision  
2/27/1997 031Labeling Revision Review 
2/28/1995 029New Dosage Regimen  
7/30/1996 028New or Modified Indication  
10/18/1978 000Approval  
 
Therapeutic Equivalents
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