QUINIDINE SULFATE Detail

Drug Name(s):
QUINIDINE SULFATE

FDA Application No.:
NDA 088072

Active Ingredient(s):
QUINIDINE SULFATE

Company:
SANDOZ

Original Approval or Tentative Approval Date:
September 25, 1983

Products on Application NDA 088072:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
QUINIDINE SULFATE	300MG	TABLET; ORAL	Prescription	AB

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January 2009

QUINIDINE SULFATE Detail

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