TAGAMET Detail

Drug Name(s):
TAGAMET

FDA Application No.:
NDA 017920

Active Ingredient(s):
CIMETIDINE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
March 16, 1978

Products on Application NDA 017920:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CIMETIDINE	200MG	TABLET; ORAL	Prescription	AB
CIMETIDINE	400MG	TABLET; ORAL	Prescription	AB

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last updated on 11-21-2008

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