Visitor Monitoring Drug Details: ACCUPRIL
 
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Drug Details

Drug Name: ACCUPRIL
FDA Application No: (NDA) 019885
Active Ingredient(s): QUINAPRIL HYDROCHLORIDE
Company: PFIZER PHARMS
Original Approval or Tentative Approval Date: November 19, 1991
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
ACCUPRIL QUINAPRIL HYDROCHLORIDEEQ 5MG BASETABLET; ORAL Prescription No AB
ACCUPRIL QUINAPRIL HYDROCHLORIDEEQ 10MG BASETABLET; ORAL Prescription No AB
ACCUPRIL QUINAPRIL HYDROCHLORIDEEQ 20MG BASETABLET; ORAL Prescription No AB
ACCUPRIL QUINAPRIL HYDROCHLORIDEEQ 40MG BASETABLET; ORAL Prescription Yes AB


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