NALOXONE HYDROCHLORIDE Detail

Drug Name(s):
NALOXONE HYDROCHLORIDE

FDA Application No.:
NDA 070172

Active Ingredient(s):
NALOXONE HYDROCHLORIDE

Company:
HOSPIRA

Original Approval or Tentative Approval Date:
April 17, 1986

Products on Application NDA 070172:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALOXONE HYDROCHLORIDE	0.4MG/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-01-2008