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Ondansetron

NDC 16714-160 · NorthStar Rx LLC

Generic nameOndansetron
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength8 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

16714-160-01 — 30 TABLET, FILM COATED in 1 BOTTLE (16714-160-01)

Billed under HCPCS

Q0162 — Ondansetron 1 mg, oral, fda approved prescription anti-emetic, for use as a complete therapeutic substitute for an iv anti-emetic at the time of chemotherapy treatment, not to exceed a 48 hour dosage regimen Medicare Part B payment limit (ASP + 6%): $0.02

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0409-4755 — ONDANSETRON, 0409-4759 — ONDANSETRON, 0615-8185 — ondansetron hydrochloride, 0641-6078 — Ondansetron, 0641-6079 — Ondansetron, 0641-6080 — Ondansetron, 0641-6286 — Ondansetron, 0904-6551 — ondansetron hydrochloride, 0904-6552 — ondansetron hydrochloride, 16714-159 — 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, 36000-012 — ONDANSETRON HYDROCHLORIDE, 42708-044 — 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.