NALOXONE Detail

Drug Name(s):
NALOXONE

FDA Application No.:
NDA 070189

Active Ingredient(s):
NALOXONE HYDROCHLORIDE

Company:
WYETH AYERST

Original Approval or Tentative Approval Date:
January 21, 1988

Products on Application NDA 070189:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALOXONE HYDROCHLORIDE	0.02MG/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008

NALOXONE Detail

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