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Ondansetron Hydrochloride

NDC 50090-4671 · A-S Medication Solutions

Generic nameOndansetron Hydrochloride
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

50090-4671-0 — 4 TABLET, FILM COATED in 1 BOTTLE (50090-4671-0)

50090-4671-1 — 10 TABLET, FILM COATED in 1 BOTTLE (50090-4671-1)

50090-4671-2 — 3 TABLET, FILM COATED in 1 BOTTLE (50090-4671-2)

50090-4671-3 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-4671-3)

50090-4671-4 — 6 TABLET, FILM COATED in 1 BOTTLE (50090-4671-4)

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.

23155-550 — ONDANSETRON, 25021-777 — ondansetron hydrochloride, 36000-012 — 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, 50090-4935 — ONDANSETRON, 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, +154 more

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