QUINAPRIL HCL Detail

Drug Name(s):
QUINAPRIL HCL

FDA Application No.:
NDA 075504

Active Ingredient(s):
QUINAPRIL HYDROCHLORIDE

Company:
TEVA

Original Approval or Tentative Approval Date:
February 7, 2002

Products on Application NDA 075504:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
QUINAPRIL HYDROCHLORIDE	EQ 10MG BASE	TABLET; ORAL	Tentative approval	none
QUINAPRIL HYDROCHLORIDE	EQ 40MG BASE	TABLET; ORAL	Tentative approval	none

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January 2009

QUINAPRIL HCL Detail

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