RANITIDINE HYDROCHLORIDE Detail

Drug Name(s):
RANITIDINE HYDROCHLORIDE

FDA Application No.:
NDA 075165

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
IVAX PHARMS

Original Approval or Tentative Approval Date:
November 22, 1999

Products on Application NDA 075165:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008