QUINIDINE GLUCONATE Detail

Drug Name(s):
QUINIDINE GLUCONATE

FDA Application No.:
NDA 089894

Active Ingredient(s):
QUINIDINE GLUCONATE

Company:
SANDOZ

Original Approval or Tentative Approval Date:
July 4, 1989

Products on Application NDA 089894:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
QUINIDINE GLUCONATE	324MG	TABLET, EXTENDED RELEASE; ORAL	Discontinued	none

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January 2009

QUINIDINE GLUCONATE Detail

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