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Ondansetron

NDC 68788-7565 · Preferred Pharmaceuticals, Inc.

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

Packages

68788-7565-1 — 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7565-1)

68788-7565-3 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7565-3)

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.

68071-4115 — Ondansetron, 68071-4570 — Ondansetron, 68071-4834 — Ondansetron, 68071-4881 — Ondansetron, 68071-5021 — Ondansetron, 68071-5167 — Ondansetron, 68071-5230 — ondansetron, 68462-157 — Ondansetron, 68462-158 — Ondansetron, 68788-4133 — Ondansetron, 68788-7644 — Ondansetron, 68788-8666 — Ondansetron, 68788-9559 — Ondansetron, 70518-1551 — Ondansetron, 70518-3512 — Ondansetron, 70518-4685 — Ondansetron, 71205-713 — Ondansetron, 71335-0650 — Ondansetron, 71335-1071 — Ondansetron, 71335-1314 — Ondansetron, +78 more

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