Visitor Monitoring Drug History: PHISOHEX
 
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Label and Approval History

Drug Name: PHISOHEX
FDA Application No: (NDA) 006882
Active Ingredient(s): HEXACHLOROPHENE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for PHISOHEX, (NDA) 006882
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/27/2003 033Labeling Revision Letter 
12/19/2001 032Control Supplement  
4/3/1990 031Labeling Revision  
7/17/1989 030Labeling Revision  
12/7/1989 029Manufacturing Change or Addition  
3/23/1988 028Control Supplement  
11/5/1982 027Package Change  
4/9/1984 026Practioner Draft Labeling  
5/15/1981 025Package Change  
2/21/1975 016Labeling Revision  
4/19/1949 000Approval  
 
Therapeutic Equivalents
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