Ondansetron Hydrochloride

NDC 57237-076 · Rising Pharma Holdings, 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

57237-076-30 — 30 TABLET, FILM COATED in 1 BOTTLE (57237-076-30)

57237-076-50 — 500 TABLET, FILM COATED in 1 BOTTLE (57237-076-50)

FDA lists these products with the same active ingredient.

55150-126 — Ondansetron Hydrochloride, 55154-2876 — Ondansetron, 55154-2877 — Ondansetron, 55154-3551 — ondansetron hydrochloride, 55154-4453 — ONDANSETRON HYDROCHLORIDE, 55154-6976 — ONDANSETRON, 55154-7879 — ondansetron hydrochloride, 55700-627 — Ondansetron Hydrochloride, 55700-631 — Ondansetron Hydrochloride, 57237-075 — Ondansetron Hydrochloride, 60505-6130 — ONDANSETRON, 60687-252 — Ondansetron, 60760-636 — Ondansetron Hydrochloride, 60760-658 — Ondansetron Hydrochloride, 60760-878 — Ondansetron Hydrochloride, 61919-565 — ONDANSETRON, 62135-350 — ONDANSETRON, 62135-351 — ONDANSETRON, 62135-555 — Ondansetron Hydrochloride, 62756-130 — ondansetron hydrochloride, +154 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.