Ondansetron

NDC 68001-246 · BluePoint Laboratories

Generic nameOndansetron

Dosage formTABLET, ORALLY DISINTEGRATING

RouteORAL

Active ingredient(s)ONDANSETRON

Strength4 mg/1

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

Marketing categoryANDA

Packages

68001-246-04 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68001-246-04)

68001-246-16 — 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68001-246-16)

68001-246-17 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (68001-246-17)

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.

63187-199 — Ondansetron, 63187-256 — Ondansetron, 63187-266 — Ondansetron, 63187-379 — Ondansetron, 63187-526 — Ondansetron, 63187-670 — ONDANSETRON, 63187-693 — ONDANSETRON, 63629-4306 — ONDANSETRON, 65862-390 — Ondansetron, 65862-391 — Ondansetron, 68001-247 — Ondansetron, 68071-1730 — Ondansetron, 68071-2284 — ondansetron, 68071-2718 — Ondansetron, 68071-2763 — Ondansetron, 68071-2901 — Ondansetron, 68071-3268 — Ondansetron, 68071-3926 — Ondansetron, 68071-4115 — Ondansetron, 68071-4570 — Ondansetron, +78 more

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