NALOXONE HYDROCHLORIDE Detail

Drug Name(s):
NALOXONE HYDROCHLORIDE

FDA Application No.:
NDA 070417

Active Ingredient(s):
NALOXONE HYDROCHLORIDE

Company:
INTL MEDICATION

Original Approval or Tentative Approval Date:
May 19, 1988

Products on Application NDA 070417:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALOXONE HYDROCHLORIDE	0.4MG/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008