LAMICTAL Detail

Drug Name(s):
LAMICTAL

FDA Application No.:
NDA 020241

Active Ingredient(s):
LAMOTRIGINE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
December 26, 1994

Products on Application NDA 020241:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LAMOTRIGINE	150MG	TABLET; ORAL	Prescription	AB
LAMOTRIGINE	250MG	TABLET; ORAL	Discontinued	none
LAMOTRIGINE	50MG	TABLET; ORAL	Discontinued	none

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last updated on 11-21-2008

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