Visitor Monitoring Drug Details: BENAZEPRIL HYDROCHLORIDE
 
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Drug Details

Drug Name: BENAZEPRIL HYDROCHLORIDE
FDA Application No: (ANDA) 076476
Active Ingredient(s): BENAZEPRIL HYDROCHLORIDE
Company: GENPHARM
Original Approval or Tentative Approval Date: February 11, 2004
 
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
BENAZEPRIL HYDROCHLORIDE BENAZEPRIL HYDROCHLORIDE5MGTABLET; ORAL Prescription No AB
BENAZEPRIL HYDROCHLORIDE BENAZEPRIL HYDROCHLORIDE10MGTABLET; ORAL Prescription No AB
BENAZEPRIL HYDROCHLORIDE BENAZEPRIL HYDROCHLORIDE20MGTABLET; ORAL Prescription No AB
BENAZEPRIL HYDROCHLORIDE BENAZEPRIL HYDROCHLORIDE40MGTABLET; ORAL Prescription No AB


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