ONDANSETRON HYDROCHLORIDE

NDC 36000-012 · Baxter Healthcare Corporation

Generic nameONDANSETRON HYDROCHLORIDE

Dosage formSOLUTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)ONDANSETRON HYDROCHLORIDE

Strength2 mg/mL

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

Marketing categoryANDA

Packages

36000-012-25 — 25 VIAL, SINGLE-DOSE in 1 CARTON (36000-012-25) / 2 mL in 1 VIAL, SINGLE-DOSE

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.

16714-159 — Ondansetron, 16714-160 — Ondansetron, 16714-671 — Ondansetron Hydrochloride, 17856-0672 — Ondansetron Hydrochloride, 17856-0691 — Ondansetron, 23155-547 — ONDANSETRON, 23155-548 — ONDANSETRON, 23155-549 — ONDANSETRON, 23155-550 — ONDANSETRON, 25021-777 — ondansetron hydrochloride, 42708-044 — Ondansetron Hydrochloride, 42708-059 — Ondansetron Hydrochloride, 42708-179 — Ondansetron Hydrochloride, 43063-770 — Ondansetron, 43063-792 — Ondansetron Hydrochloride, 50090-3178 — Ondansetron Hydrochloride, 50090-3185 — Ondansetron Hydrochloride, 50090-4671 — Ondansetron Hydrochloride, 50090-4935 — ONDANSETRON, 50090-6342 — 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.