Visitor Monitoring Drug History: BACTROBAN
 
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: BACTROBAN
FDA Application No: (NDA) 050703
Active Ingredient(s): MUPIROCIN CALCIUM
Company: GLAXOSMITHKLINE
 
Label History
 
Labels are not available on this site for BACTROBAN, (NDA) 050703
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/15/2001 008Control Supplement  
11/9/2001 007Control Supplement  
12/13/2000 006Manufacturing Change or Addition  
10/6/1999 005Manufacturing Change or Addition  
5/19/1999 004Control Supplement  
9/4/1998 003Manufacturing Change or Addition  
4/3/1996 002Control Supplement  
11/20/1995 001Manufacturing Change or Addition  
9/18/1995 000Approval  
 
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