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ondansetron

NDC 55154-7879 · Cardinal Health 107, LLC

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

55154-7879-0 — 10 BLISTER PACK in 1 BAG (55154-7879-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55111-154 — ONDANSETRON HYDROCHLORIDE, 55111-155 — ondansetron hydrochloride, 55111-156 — ONDANSETRON HYDROCHLORIDE, 55150-125 — Ondansetron Hydrochloride, 55150-126 — Ondansetron Hydrochloride, 55154-2876 — Ondansetron, 55154-2877 — Ondansetron, 55154-3551 — ondansetron hydrochloride, 55154-4453 — ONDANSETRON HYDROCHLORIDE, 55154-6976 — ONDANSETRON, 55700-627 — Ondansetron Hydrochloride, 55700-631 — Ondansetron Hydrochloride, 57237-075 — Ondansetron Hydrochloride, 57237-076 — Ondansetron Hydrochloride, 60505-6130 — ONDANSETRON, 60687-252 — Ondansetron, 60760-636 — Ondansetron Hydrochloride, 60760-658 — Ondansetron Hydrochloride, 60760-878 — Ondansetron Hydrochloride, 61919-565 — ONDANSETRON, +154 more

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