NALOXONE Detail

Drug Name(s):
NALOXONE

FDA Application No.:
NDA 070191

Active Ingredient(s):
NALOXONE HYDROCHLORIDE

Company:
WYETH AYERST

Original Approval or Tentative Approval Date:
October 1, 1985

Products on Application NDA 070191:

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

NALOXONE Detail

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