TAGAMET Detail

Drug Name(s):
TAGAMET

FDA Application No.:
NDA 017939

Active Ingredient(s):
CIMETIDINE HYDROCHLORIDE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
December 26, 1977

Products on Application NDA 017939:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CIMETIDINE HYDROCHLORIDE	EQ 300MG BASE/2ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 11-21-2008

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