LARIAM Detail

Drug Name(s):
LARIAM

FDA Application No.:
NDA 019591

Active Ingredient(s):
MEFLOQUINE HYDROCHLORIDE

Company:
ROCHE

Original Approval or Tentative Approval Date:
May 1, 1989

Products on Application NDA 019591:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MEFLOQUINE HYDROCHLORIDE	250MG	TABLET; ORAL	Prescription	AB

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last updated on 11-21-2008

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