Visitor Monitoring Drug History: BENOQUIN
 
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: BENOQUIN
FDA Application No: (NDA) 008173
Active Ingredient(s): MONOBENZONE
Company: VALEANT PHARM INTL
 
Label History
 
View the label approved on March 28, 2003 for BENOQUIN, (NDA) 008173


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/26/2003 015Labeling Revision Letter
Label 
3/16/1998 014Manufacturing Change or Addition  
11/7/1997 013Control Supplement  
9/23/1997 012Control Supplement  
4/3/1997 011Control Supplement  
1/31/1997 010Control Supplement  
1/17/1995 009Labeling Revision  
4/27/1993 008Formulation Revision  
4/27/1993 007Manufacturing Change or Addition  
8/8/1984 006Labeling Revision  
11/10/1952 000Approval  
 
There are no Therapeutic Equivalents
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