Visitor Monitoring Drug History: HIBICLENS
 
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: HIBICLENS
FDA Application No: (NDA) 017768
Active Ingredient(s): CHLORHEXIDINE GLUCONATE
Company: REGENT
 
Label History
 
Labels are not available on this site for HIBICLENS, (NDA) 017768
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/2/2002 033Manufacturing Change or Addition  
12/12/2001 032Manufacturing Change or Addition  
2/23/2000 031Package Change  
10/20/1999 030Package Change  
9/30/1998 029Control Supplement  
3/30/1994 028Package Change  
7/14/1989 027Formulation Revision  
7/18/1989 026Control Supplement  
8/25/1989 025Labeling Revision  
5/11/1988 024Manufacturing Change or Addition  
3/3/1988 023Labeling Revision  
4/6/1987 022Package Change  
5/9/1985 019Control Supplement  
6/18/1984 017Manufacturing Change or Addition  
7/21/1981 015Control Supplement  
3/10/1981 014Control Supplement  
1/16/1981 013Package Change  
12/29/1980 012Control Supplement  
5/20/1987 011Labeling Revision  
7/30/1980 010Formulation Revision  
7/25/1979 008Package Change  
12/18/1979 007Formulation Revision  
12/18/1979 006Manufacturing Change or Addition  
7/6/1981 005Labeling Revision  
5/12/1978 004Control Supplement  
1/6/1978 003Manufacturing Change or Addition  
3/1/1982 002General Efficacy (MarkIV)  
5/9/1977 001Control Supplement  
9/17/1976 000Approval  
 
Therapeutic Equivalents
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