ZANTAC 300 Detail

Drug Name(s):
ZANTAC 300

FDA Application No.:
NDA 018703

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
January 4, 1984

Products on Application NDA 018703:

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 11-21-2008

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