ZANTAC 150 Detail

Drug Name(s):
ZANTAC 150

FDA Application No.:
NDA 021698

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
PFIZER CONS HLTHCARE

Original Approval or Tentative Approval Date:
August 30, 2004

Products on Application NDA 021698:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET; ORAL	OTC	none

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last updated on 11-21-2008

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