BACLOFEN Detail

Drug Name(s):
BACLOFEN

FDA Application No.:
NDA 074584

Active Ingredient(s):
BACLOFEN

Company:
USL PHARMA

Original Approval or Tentative Approval Date:
August 18, 1996

Products on Application NDA 074584:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BACLOFEN	10MG	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008

BACLOFEN Detail

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