QUINAPRIL HYDROCHLORIDE Detail

Drug Name(s):
QUINAPRIL HYDROCHLORIDE

FDA Application No.:
NDA 076049

Active Ingredient(s):
QUINAPRIL HYDROCHLORIDE

Company:
ANDRX PHARMS

Original Approval or Tentative Approval Date:
January 13, 2005

Products on Application NDA 076049:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
QUINAPRIL HYDROCHLORIDE	EQ 20MG BASE	TABLET; ORAL	Prescription	AB
QUINAPRIL HYDROCHLORIDE	EQ 5MG BASE	TABLET; ORAL	Prescription	AB

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January 2009

QUINAPRIL HYDROCHLORIDE Detail

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