Visitor Monitoring Drug History: BENEMID
 
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: BENEMID
FDA Application No: (NDA) 007898
Active Ingredient(s): PROBENECID
Company: MERCK
 
Label History
 
Labels are not available on this site for BENEMID, (NDA) 007898
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/23/1998 045Labeling Revision  
1/11/1995 044Manufacturing Change or Addition  
8/18/1994 043Control Supplement  
4/20/1994 042Control Supplement  
11/30/1989 041Manufacturing Change or Addition  
5/3/1988 040Manufacturing Change or Addition  
4/23/1998 039Labeling Revision  
5/12/1988 038Labeling Revision  
5/12/1988 036Labeling Revision  
5/12/1988 035Labeling Revision  
7/23/1985 032Manufacturing Change or Addition  
3/2/1982 031Manufacturing Change or Addition  
3/8/1984 030Package Change  
2/24/1979 026Manufacturing Change or Addition  
2/5/1979 025Labeling Revision  
1/25/1979 023Final Printed Labeling - MarkIV  
6/1/1978 022Labeling Revision  
9/22/1978 021Control Supplement  
12/3/1979 019Package Change  
10/11/1978 018Control Supplement  
8/26/1977 017Labeling Revision  
4/8/1977 016Supplement  
6/28/1976 015Labeling Revision  
6/28/1976 014Other Amendment  
4/26/1951 000Approval  
 
Therapeutic Equivalents
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