RANITIDINE Detail

Drug Name(s):
RANITIDINE

FDA Application No.:
NDA 075132

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
RANBAXY

Original Approval or Tentative Approval Date:
June 28, 2000

Products on Application NDA 075132:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
RANITIDINE HYDROCHLORIDE	EQ 75MG BASE	TABLET; ORAL	OTC	none

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last updated on 12-01-2008

RANITIDINE Detail

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