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Ondansetron Hydrochloride

NDC 68071-4705 · NuCare Pharmaceuticals,Inc.

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

68071-4705-4 — 4 TABLET, FILM COATED in 1 BOTTLE (68071-4705-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67184-0507 — ONDANSETRON, 67296-1562 — Ondansetron Hydrochloride, 67296-2119 — Ondansetron, 67877-170 — Ondansetron Hydrochloride, 68071-1742 — Ondansetron Hydrochloride, 68071-2053 — Ondansetron Hydrochloride, 68071-3611 — Ondansetron Hydrochloride, 68071-3713 — Ondansetron, 68071-3801 — Ondansetron, 68071-4328 — Ondansetron Hydrochloride, 68071-4966 — Ondansetron Hydrochloride, 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, +154 more

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