Last Updated: November 8, 2026

Details for New Drug Application (NDA): 074471

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NDA 074471 describes NALBUPHINE HYDROCHLORIDE, which is a drug marketed by Abbvie, Abbott, Abraxis Pharm, Dr Reddys, Hospira, Igi Labs Inc, Rising, and Somerset Theraps Llc, and is included in eighteen NDAs. It is available from six suppliers. Additional details are available on the NALBUPHINE HYDROCHLORIDE profile page.

The generic ingredient in NALBUPHINE HYDROCHLORIDE is nalbuphine hydrochloride. There is one drug master file entry for this compound. Six suppliers are listed for this compound. Additional details are available on the nalbuphine hydrochloride profile page.

Summary for 074471

Tradename:	NALBUPHINE HYDROCHLORIDE
Applicant:	Dr Reddys
Ingredient:	nalbuphine hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 074471

Analgesics, Opioid
Narcotic Antagonists
Narcotics

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS			Strength	100MG/10ML (10MG/ML)
Approval Date:	Mar 19, 1998	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS			Strength	200MG/10ML (20MG/ML)
Approval Date:	Mar 19, 1998	TE:		RLD:	No

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