BACLOFEN Detail

Drug Name(s):
BACLOFEN

FDA Application No.:
NDA 077121

Active Ingredient(s):
BACLOFEN

Company:
ALPHAPHARM

Original Approval or Tentative Approval Date:
July 28, 2005

Products on Application NDA 077121:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BACLOFEN	20MG	TABLET; ORAL	Prescription	none

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last updated on 11-19-2008

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