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) 050591
Active Ingredient(s): MUPIROCIN
Company: GLAXOSMITHKLINE
 
Label History
 
Labels are not available on this site for BACTROBAN, (NDA) 050591
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/9/2001 026Control Supplement  
9/21/2001 025Control Supplement  
9/12/2000 024Package Change  
5/19/1999 023Control Supplement  
4/22/1999 022Efficacy Supplement with Clinical Data to Support Letter
Review 
12/3/1997 021Manufacturing Change or Addition  
12/24/1996 020Manufacturing Change or Addition  
6/6/1996 019Control Supplement  
11/2/1993 018Expiration Date Change  
3/24/1994 017Package Change  
3/24/1994 016Manufacturing Change or Addition  
2/21/1996 015Labeling Revision  
4/15/1991 013Labeling Revision  
9/30/1991 012Labeling Revision  
4/15/1991 011Labeling Revision  
4/15/1991 010Labeling Revision  
4/15/1991 009Labeling Revision  
12/31/1987 000Approval  
 
Therapeutic Equivalents
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