Visitor Monitoring Drug Details: QUINARETIC
 
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Drug Details

Drug Name: QUINARETIC
FDA Application No: (ANDA) 076374
Active Ingredient(s): HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Company: ACTAVIS TOTOWA
Original Approval or Tentative Approval Date: March 31, 2004
 
There are no 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
QUINARETIC HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE12.5MG; EQ 10MG BASETABLET; ORAL Prescription No AB
QUINARETIC HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE12.5MG; EQ 20MG BASETABLET; ORAL Prescription No AB
QUINARETIC HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE25MG; EQ 20MG BASETABLET; ORAL Prescription No AB


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