ZONISAMIDE Detail

Drug Name(s):
ZONISAMIDE

FDA Application No.:
NDA 077639

Active Ingredient(s):
ZONISAMIDE

Company:
BARR

Original Approval or Tentative Approval Date:
December 21, 2005

Products on Application NDA 077639:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ZONISAMIDE	50MG	CAPSULE; ORAL	Prescription	AB

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last updated on 12-05-2008

ZONISAMIDE Detail

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