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Ondansetron Hydrochloride

NDC 72162-2364 · Bryant Ranch Prepack

Generic nameOndansetron Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength4 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

72162-2364-5 — 500 TABLET, FILM COATED in 1 BOTTLE (72162-2364-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-0205 — Ondansetron Hydrochloride, 71335-0815 — ondansetron hydrochloride, 71335-1357 — Ondansetron Hydrochloride, 71335-1596 — Ondansetron Hydrochloride, 71335-1855 — Ondansetron Hydrochloride, 71610-119 — Ondansetron Hydrochloride, 71872-7068 — ONDANSETRON, 71872-7107 — Ondansetron, 71872-7140 — Ondansetron, 71872-7162 — ONDANSETRON, 72162-2365 — Ondansetron Hydrochloride, 72266-123 — Ondansetron, 72266-124 — Ondansetron, 72572-520 — Ondansetron, 72789-034 — Ondansetron Hydrochloride, 76045-103 — ONDANSETRON HYDROCHLORIDE, 76045-216 — ONDANSETRON HYDROCHLORIDE, 76420-915 — Ondansetron Hydrochloride, 76420-916 — Ondansetron Hydrochloride, 76420-917 — 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.