NALBUPHINE Detail

Drug Name(s):
NALBUPHINE

FDA Application No.:
NDA 070751

Active Ingredient(s):
NALBUPHINE HYDROCHLORIDE

Company:
ABRAXIS PHARM

Products on Application NDA 070751:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALBUPHINE HYDROCHLORIDE	10MG/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008

NALBUPHINE Detail

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