Visitor Monitoring Drug Details: QUINAPRIL HYDROCHLORIDE
 
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Drug Details

Drug Name: QUINAPRIL HYDROCHLORIDE
FDA Application No: (ANDA) 076651
Active Ingredient(s): QUINAPRIL HYDROCHLORIDE
Company: MUTUAL PHARMA
Original Approval or Tentative Approval Date: July 15, 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
QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE5MGTABLET; ORAL Tentative Approval No None
QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE10MGTABLET; ORAL Tentative Approval No None
QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE20MGTABLET; ORAL Tentative Approval No None
QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE40MGTABLET; ORAL Tentative Approval No None


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