Visitor Monitoring Drug History: VERMOX
 
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Label and Approval History

Drug Name: VERMOX
FDA Application No: (NDA) 017481
Active Ingredient(s): MEBENDAZOLE
Company: MCNEIL PED
 
Label History
 
Labels are not available on this site for VERMOX, (NDA) 017481
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/20/1998 045Control Supplement  
7/27/1998 044Package Change  
5/20/1998 043Control Supplement  
3/20/1998 042Manufacturing Change or Addition  
9/27/1995 041Manufacturing Change or Addition  
6/16/1994 040Control Supplement  
2/13/1998 038Labeling Revision  
12/23/1993 037Control Supplement  
1/28/1993 036Manufacturing Change or Addition  
1/28/1993 035Manufacturing Change or Addition  
9/28/1989 034Labeling Revision  
1/26/1986 032Control Supplement  
8/9/1984 031Manufacturing Change or Addition  
8/31/1984 029Manufacturing Change or Addition  
5/14/1984 028Labeling Revision  
3/16/1983 027Manufacturing Change or Addition  
3/16/1983 026Manufacturing Change or Addition  
7/11/1983 025Labeling Revision  
6/4/1981 024Control Supplement  
12/29/1980 023Control Supplement  
4/3/1980 020Formulation Revision  
4/1/1980 019Manufacturing Change or Addition  
4/1/1980 018Manufacturing Change or Addition  
3/8/1979 016Labeling Revision  
3/8/1979 014Manufacturing Change or Addition  
9/13/1979 013Manufacturing Change or Addition  
2/15/1979 012Manufacturing Change or Addition  
10/27/1978 011Manufacturing Change or Addition  
4/24/1978 010Manufacturing Change or Addition  
8/24/1977 009Labeling Revision  
7/29/1977 008Labeling Revision  
3/4/1977 007Labeling Revision  
3/18/1976 006Labeling Revision  
10/30/1975 005Control Supplement  
10/30/1975 004Control Supplement  
3/18/1976 003Control Supplement  
6/28/1974 000Approval  
 
Therapeutic Equivalents
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