Visitor Monitoring Drug History: HIBISTAT
 
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: HIBISTAT
FDA Application No: (NDA) 018300
Active Ingredient(s): CHLORHEXIDINE GLUCONATE
Company: REGENT
 
Label History
 
Labels are not available on this site for HIBISTAT, (NDA) 018300
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/13/2004 015Manufacturing Change or Addition Letter 
1/13/2004 014Manufacturing Change or Addition Letter 
2/18/2000 013Package Change  
10/19/1999 012Package Change  
4/9/1996 011Manufacturing Change or Addition  
4/14/1994 010Package Change  
12/22/1992 009Manufacturing Change or Addition  
9/15/1989 008Manufacturing Change or Addition  
5/9/1988 007Manufacturing Change or Addition  
8/4/1989 006Labeling Revision  
3/4/1985 005Package Change  
3/10/1981 004Control Supplement  
1/16/1981 003Manufacturing Change or Addition  
12/29/1980 002Control Supplement  
6/26/1980 001Package Change  
5/23/1980 000Approval  
 
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