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Ondansetron Hydrochloride

NDC 68788-9368 · Preferred Pharmaceuticals, Inc.

Generic nameOndansetron Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength4 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

68788-9368-1 — 10 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1)

68788-9368-2 — 12 TABLET, FILM COATED in 1 BOTTLE (68788-9368-2)

68788-9368-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-9368-3)

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.

68071-5047 — Ondansetron Hydrochloride, 68083-113 — Ondansetron, 68083-114 — Ondansetron, 68084-220 — Ondansetron Hydrochloride, 68084-221 — Ondansetron Hydrochloride, 68094-763 — Ondansetron Hydrochloride, 68462-105 — Ondansetron, 68462-106 — Ondansetron, 68788-8582 — Ondansetron Hydrochloride, 68788-8651 — Ondansetron Hydrochloride, 68788-9402 — Ondansetron Hydrochloride, 68999-555 — Ondansetron Hydrochloride, 69339-171 — Ondansetron, 69339-172 — Ondansetron, 70518-1585 — Ondansetron Hydrochloride, 70518-3511 — Ondansetron Hydrochloride, 70518-4145 — Ondansetron Hydrochloride, 70518-4245 — Ondansetron, 70518-4588 — Ondansetron, 71205-744 — Ondansetron Hydrochloride, +154 more

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