Ondansetron

NDC 43063-770 · PD-Rx 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

43063-770-06 — 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-770-06)

FDA lists these products with the same active ingredient.

17856-0691 — Ondansetron, 23155-547 — ONDANSETRON, 23155-548 — ONDANSETRON, 23155-549 — ONDANSETRON, 23155-550 — ONDANSETRON, 25021-777 — ondansetron hydrochloride, 36000-012 — ONDANSETRON HYDROCHLORIDE, 42708-044 — Ondansetron Hydrochloride, 42708-059 — Ondansetron Hydrochloride, 42708-179 — Ondansetron Hydrochloride, 43063-792 — Ondansetron Hydrochloride, 50090-3178 — Ondansetron Hydrochloride, 50090-3185 — Ondansetron Hydrochloride, 50090-4671 — Ondansetron Hydrochloride, 50090-4935 — ONDANSETRON, 50090-6342 — Ondansetron Hydrochloride, 50268-621 — Ondansetron Hydrochloride, 50268-622 — Ondansetron Hydrochloride, 50268-647 — Ondansetron, 51407-003 — 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.