Visitor Monitoring Drug Details: BENOQUIN
 
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Drug Details

Drug Name: BENOQUIN
FDA Application No: (NDA) 008173
Active Ingredient(s): MONOBENZONE
Company: VALEANT PHARM INTL
Original Approval or Tentative Approval Date: November 10, 1952
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
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