Visitor Monitoring Drug Details: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
 
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Drug Details

Drug Name: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
FDA Application No: (ANDA) 076348
Active Ingredient(s): BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Company: IVAX PHARMS
Original Approval or Tentative Approval Date: February 12, 2004
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE5MG; 6.25MGTABLET; ORAL Prescription No AB
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE10MG; 12.5MGTABLET; ORAL Prescription No AB
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE20MG; 12.5MGTABLET; ORAL Prescription No AB
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE20MG; 25MGTABLET; ORAL Prescription No AB


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