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ONDANSETRON

NDC 51662-1245 · HF Acquisition Co LLC, DBA HealthFirst

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

51662-1245-1 — 2 mL in 1 VIAL, SINGLE-DOSE (51662-1245-1)

51662-1245-3 — 25 POUCH in 1 CASE (51662-1245-3) / 1 VIAL in 1 POUCH (51662-1245-2) / 2 mL in 1 VIAL

Billed under HCPCS

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

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6342 — Ondansetron Hydrochloride, 50268-621 — Ondansetron Hydrochloride, 50268-622 — Ondansetron Hydrochloride, 50268-647 — Ondansetron, 51407-003 — Ondansetron, 51407-004 — Ondansetron, 51655-016 — Ondansetron Hydrochloride, 51655-415 — Ondansetron Hydrochloride, 51655-813 — Ondansetron Hydrochloride, 51655-933 — Ondansetron Hydrochloride, 51662-1366 — ONDANSETRON, 51662-1377 — ONDANSETRON, 51662-1469 — ONDANSETRON, 51662-1539 — ONDANSETRON, 51662-1678 — ONDANSETRON, 54348-819 — ONDANSETRON, 54348-821 — Ondansetron Hydrochloride, 55111-153 — ONDANSETRON HYDROCHLORIDE, 55111-154 — ONDANSETRON HYDROCHLORIDE, 55111-155 — 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.