Visitor Monitoring Drug History: VANCOCIN HYDROCHLORIDE
 
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: VANCOCIN HYDROCHLORIDE
FDA Application No: (NDA) 050606
Active Ingredient(s): VANCOMYCIN HYDROCHLORIDE
Company: VIROPHARMA
 
Label History
 
View the label approved on June 1, 2004 for VANCOCIN HYDROCHLORIDE, (NDA) 050606


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
5/27/2004 020Labeling Revision Letter
Label 
3/17/2004 019Approval Letter 
5/28/2002 016Expiration Date Change  
5/24/2002 015Labeling Revision Letter 
2/6/2001 014Labeling Revision  
3/18/1998 013Manufacturing Change or Addition  
5/12/1997 012Labeling Revision  
6/30/1993 010Labeling Revision  
6/14/1996 009Labeling Revision  
9/27/1995 008Labeling Revision  
6/14/1996 006Labeling Revision  
5/23/1988 005Labeling Revision  
8/18/1987 004Control Supplement  
8/12/1987 003Labeling Revision  
10/8/1986 002Formulation Revision  
6/5/1986 001Labeling Revision  
4/15/1986 000Approval  
 
There are no Therapeutic Equivalents
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