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Ondansetron Hydrochloride

NDC 68084-221 · American Health Packaging

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

68084-221-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-221-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11)

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.

68071-3611 — Ondansetron Hydrochloride, 68071-3713 — Ondansetron, 68071-3801 — Ondansetron, 68071-4328 — Ondansetron Hydrochloride, 68071-4705 — Ondansetron Hydrochloride, 68071-4966 — Ondansetron Hydrochloride, 68071-5047 — Ondansetron Hydrochloride, 68083-113 — Ondansetron, 68083-114 — Ondansetron, 68084-220 — Ondansetron Hydrochloride, 68094-763 — Ondansetron Hydrochloride, 68462-105 — Ondansetron, 68462-106 — Ondansetron, 68788-8582 — Ondansetron Hydrochloride, 68788-8651 — Ondansetron Hydrochloride, 68788-9368 — Ondansetron Hydrochloride, 68788-9402 — Ondansetron Hydrochloride, 68999-555 — Ondansetron Hydrochloride, 69339-171 — Ondansetron, 69339-172 — Ondansetron, +154 more

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