Ondansetron

NDC 72266-123 · Fosun Pharma USA Inc.

Generic nameOndansetron

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)ONDANSETRON HYDROCHLORIDE

Strength2 mg/mL

Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

Marketing categoryANDA

Packages

72266-123-25 — 25 VIAL in 1 CARTON (72266-123-25) / 2 mL in 1 VIAL (72266-123-01)

J2405 — Injection, ondansetron hydrochloride, per 1 mg Medicare Part B payment limit (ASP + 6%): $0.09

FDA lists these products with the same active ingredient.

71335-1357 — Ondansetron Hydrochloride, 71335-1596 — Ondansetron Hydrochloride, 71335-1855 — Ondansetron Hydrochloride, 71610-119 — Ondansetron Hydrochloride, 71872-7068 — ONDANSETRON, 71872-7107 — Ondansetron, 71872-7140 — Ondansetron, 71872-7162 — ONDANSETRON, 72162-2364 — Ondansetron Hydrochloride, 72162-2365 — Ondansetron Hydrochloride, 72266-124 — Ondansetron, 72572-520 — Ondansetron, 72789-034 — Ondansetron Hydrochloride, 76045-103 — ONDANSETRON HYDROCHLORIDE, 76045-216 — ONDANSETRON HYDROCHLORIDE, 76420-915 — Ondansetron Hydrochloride, 76420-916 — Ondansetron Hydrochloride, 76420-917 — Ondansetron Hydrochloride, 80425-0072 — Ondansetron HCL, 80425-0074 — Ondansetron HCL, +154 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.