Drug Details: NALBUPHINE HYDROCHLORIDE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	NALBUPHINE HYDROCHLORIDE
FDA Application No:	(NDA) 020200
Active Ingredient(s):	NALBUPHINE HYDROCHLORIDE
Company:	ABBOTT
Original Approval or Tentative Approval Date:	March 12, 1993
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

There are no Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
NALBUPHINE HYDROCHLORIDE	NALBUPHINE HYDROCHLORIDE	1.5MG/ML	INJECTABLE; INJECTION	Discontinued	No	None

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