LAMOTRIGINE Detail

Drug Name(s):
LAMOTRIGINE

FDA Application No.:
NDA 076420

Active Ingredient(s):
LAMOTRIGINE

Company:
TEVA

Original Approval or Tentative Approval Date:
June 20, 2006

Products on Application NDA 076420:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LAMOTRIGINE	25MG	TABLET, CHEWABLE; ORAL	Prescription	AB

Recall Notices

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January 2009

LAMOTRIGINE Detail

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