Visitor Monitoring Drug History: VANTIN
 
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: VANTIN
FDA Application No: (NDA) 050674
Active Ingredient(s): CEFPODOXIME PROXETIL
Company: PHARMACIA AND UPJOHN
 
Label History
 
View the label approved on June 7, 2007 for VANTIN, (NDA) 050674


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 014Labeling Revision Letter
Label 
6/2/2004 013Labeling Revision Letter
Label 
11/20/1998 012New or Modified Indication Letter
Review 
2/7/1996 010Labeling Revision  
9/28/1995 009Labeling Revision  
3/14/1996 008Labeling Revision  
3/14/1996 007New or Modified Indication  
5/7/1996 005New Dosage Regimen  
7/6/1994 004Labeling Revision  
11/2/1993 003Labeling Revision  
4/8/1993 002Labeling Revision  
5/28/1993 001New or Modified Indication  
8/7/1992 000Approval  
 
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