QUINIDINE SULFATE Detail

Drug Name(s):
QUINIDINE SULFATE

FDA Application No.:
NDA 087011

Active Ingredient(s):
QUINIDINE SULFATE

Company:
CLONMEL HLTHCARE

Original Approval or Tentative Approval Date:
August 28, 1979

Products on Application NDA 087011:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
QUINIDINE SULFATE	200MG	TABLET; ORAL	Discontinued	none

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January 2009

QUINIDINE SULFATE Detail

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