TEGRETOL Detail

Drug Name(s):
TEGRETOL

FDA Application No.:
NDA 016608

Active Ingredient(s):
CARBAMAZEPINE

Company:
NOVARTIS

Original Approval or Tentative Approval Date:
July 14, 1974

Products on Application NDA 016608:

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

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last updated on 11-21-2008

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