RANITIDINE Detail

Drug Name(s):
RANITIDINE

FDA Application No.:
NDA 075439

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
RANBAXY

Original Approval or Tentative Approval Date:
November 8, 2000

Products on Application NDA 075439:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 11-19-2008

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