BACLOFEN Detail

Drug Name(s):
BACLOFEN

FDA Application No.:
NDA 077241

Active Ingredient(s):
BACLOFEN

Company:
LANNETT

Original Approval or Tentative Approval Date:
December 19, 2005

Products on Application NDA 077241:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BACLOFEN	20MG	TABLET; ORAL	Prescription	AB

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last updated on 12-05-2008

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