Visitor Monitoring Drug History: EXIDINE
 
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: EXIDINE
FDA Application No: (NDA) 019422
Active Ingredient(s): CHLORHEXIDINE GLUCONATE
Company: XTTRIUM
 
Label History
 
Labels are not available on this site for EXIDINE, (NDA) 019422
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/20/2004 033Package Change Letter 
12/19/2003 032Efficacy Supplement with Clinical Data to Support Letter
Review 
10/8/1999 029Package Change  
3/29/2000 028Package Change  
10/19/1998 027Control Supplement  
9/30/1998 026Package Change  
1/8/1998 025Control Supplement  
4/17/1997 024Package Change  
3/11/1997 023Expiration Date Change  
5/6/1996 022Package Change  
4/3/1996 021Control Supplement  
2/12/1996 020Formulation Revision  
2/6/1996 019Control Supplement  
2/6/1996 018Control Supplement  
5/10/1995 017Manufacturing Change or Addition  
5/10/1995 016Package Change  
11/6/1992 015Package Change  
7/28/1989 009Manufacturing Change or Addition  
8/12/1988 007Manufacturing Change or Addition  
6/28/1988 006Control Supplement  
4/12/1988 005Expiration Date Change  
9/16/1987 004Manufacturing Change or Addition  
9/16/1987 003Package Change  
3/2/1988 002Package Change  
12/27/1989 001New or Modified Indication  
12/17/1985 000Approval  
 
Therapeutic Equivalents
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