Ondansetron

NDC 71872-7140 · Medical Purchasing Solutions, LLC

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

71872-7140-1 — 1 VIAL in 1 BAG (71872-7140-1) / 2 mL in 1 VIAL

FDA lists these products with the same active ingredient.

71205-744 — Ondansetron Hydrochloride, 71335-0132 — Ondansetron, 71335-0205 — Ondansetron Hydrochloride, 71335-0815 — ondansetron hydrochloride, 71335-1357 — Ondansetron Hydrochloride, 71335-1596 — Ondansetron Hydrochloride, 71335-1855 — Ondansetron Hydrochloride, 71610-119 — Ondansetron Hydrochloride, 71872-7068 — ONDANSETRON, 71872-7107 — Ondansetron, 71872-7162 — ONDANSETRON, 72162-2364 — Ondansetron Hydrochloride, 72162-2365 — Ondansetron Hydrochloride, 72266-123 — Ondansetron, 72266-124 — Ondansetron, 72572-520 — Ondansetron, 72789-034 — Ondansetron Hydrochloride, 76045-103 — ONDANSETRON HYDROCHLORIDE, 76045-216 — ONDANSETRON HYDROCHLORIDE, 76420-915 — Ondansetron Hydrochloride, +154 more

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