NALTREXONE HYDROCHLORIDE Detail

Drug Name(s):
NALTREXONE HYDROCHLORIDE

FDA Application No.:
NDA 074918

Active Ingredient(s):
NALTREXONE HYDROCHLORIDE

Company:
BARR

Original Approval or Tentative Approval Date:
November 30, 1998

Products on Application NDA 074918:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALTREXONE HYDROCHLORIDE	50MG	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008