RANITIDINE HYDROCHLORIDE Detail

Drug Name(s):
RANITIDINE HYDROCHLORIDE

FDA Application No.:
NDA 075564

Active Ingredient(s):
RANITIDINE HYDROCHLORIDE

Company:
GENPHARM

Original Approval or Tentative Approval Date:
October 26, 2000

Products on Application NDA 075564:

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

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last updated on 11-19-2008

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