NALBUPHINE HYDROCHLORIDE Detail

Drug Name(s):
NALBUPHINE HYDROCHLORIDE

FDA Application No.:
NDA 070917

Active Ingredient(s):
NALBUPHINE HYDROCHLORIDE

Company:
ABBOTT

Original Approval or Tentative Approval Date:
February 2, 1989

Products on Application NDA 070917:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALBUPHINE HYDROCHLORIDE	20MG/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008