RANITIDINE HYDROCHLORIDE Detail

Drug Name(s):
RANITIDINE HYDROCHLORIDE

FDA Application No.:
NDA 075000

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
RANBAXY

Original Approval or Tentative Approval Date:
January 29, 1998

Products on Application NDA 075000:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET; ORAL	Discontinued	none

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last updated on 12-01-2008