ZANTAC IN PLASTIC CONTAINER Detail

Drug Name(s):
ZANTAC IN PLASTIC CONTAINER

FDA Application No.:
NDA 019593

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
May 17, 1987

Products on Application NDA 019593:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
RANITIDINE HYDROCHLORIDE	EQ 1MG BASE/ML	INJECTABLE; INJECTION	Prescription	none

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last updated on 11-21-2008

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