Drug History: NALBUPHINE HYDROCHLORIDE

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	NALBUPHINE HYDROCHLORIDE
FDA Application No:	(ANDA) 070917
Active Ingredient(s):	NALBUPHINE HYDROCHLORIDE
Company:	ABBOTT

Label History

Labels are not available on this site for NALBUPHINE HYDROCHLORIDE, (ANDA) 070917

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
4/26/1996	003	Labeling
2/28/1991	002	Labeling
7/25/1990	001	Labeling
2/3/1989	000	Approval

Therapeutic Equivalents

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