Ondansetron

NDC 68071-3801 · NuCare Pharmaceuticals, Inc.

Generic nameOndansetron

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

68071-3801-1 — 10 TABLET, FILM COATED in 1 BOTTLE (68071-3801-1)

FDA lists these products with the same active ingredient.

65862-208 — Ondansetron Hydrochloride, 67046-1242 — Ondansetron Hydrochloride, 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, 68071-4328 — Ondansetron Hydrochloride, 68071-4705 — Ondansetron Hydrochloride, 68071-4966 — Ondansetron Hydrochloride, 68071-5047 — Ondansetron Hydrochloride, 68083-113 — Ondansetron, 68083-114 — Ondansetron, 68084-220 — Ondansetron Hydrochloride, 68084-221 — Ondansetron Hydrochloride, 68094-763 — Ondansetron Hydrochloride, 68462-105 — 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.