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Nalbuphine hydrochloride

NDC 71872-7331 · Medical Purchasing Solutions, LLC

Generic nameNalbuphine hydrochloride
Dosage formINJECTION
RouteINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Active ingredient(s)NALBUPHINE HYDROCHLORIDE
Strength10 mg/mL
Pharmacologic classCompetitive Opioid Antagonists [MoA], Opioid Agonist/Antagonist [EPC], Partial Opioid Agonists [MoA]
Marketing categoryANDA

Packages

71872-7331-1 — 1 VIAL, MULTI-DOSE in 1 BAG (71872-7331-1) / 10 mL in 1 VIAL, MULTI-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0404-9766 — nalbuphine hydrochloride, 0404-9767 — nalbuphine hydrochloride, 0404-9918 — Nalbuphine Hydrochloride, 0409-1463 — NALBUPHINE HYDROCHLORIDE, 0409-1464 — NALBUPHINE HYDROCHLORIDE, 0409-1465 — NALBUPHINE HYDROCHLORIDE, 0409-1467 — NALBUPHINE HYDROCHLORIDE, 51662-1418 — NALBUPHINE HCI, 51662-1420 — NALBUPHINE HCI, 70069-661 — Nalbuphine hydrochloride, 70069-662 — Nalbuphine hydrochloride, 70069-671 — Nalbuphine hydrochloride, 70069-672 — Nalbuphine hydrochloride, 71872-7114 — NALBUPHINE HYDROCHLORIDE, 71872-7320 — NALBUPHINE HYDROCHLORIDE, 84549-464 — NALBUPHINE HYDROCHLORIDE

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.