Visitor Monitoring Drug Details: BENAZEPRIL HYDROCHLORIDE
 
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Drug Details

Drug Name: BENAZEPRIL HYDROCHLORIDE
FDA Application No: (ANDA) 076267
Active Ingredient(s): BENAZEPRIL HYDROCHLORIDE
Company: ANDRX PHARMS
Original Approval or Tentative Approval Date: February 11, 2004
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
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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