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Ondansetron

NDC 70518-4588 · REMEDYREPACK INC.

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

Packages

70518-4588-0 — 30 TABLET in 1 BLISTER PACK (70518-4588-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8651 — Ondansetron Hydrochloride, 68788-9368 — Ondansetron Hydrochloride, 68788-9402 — Ondansetron Hydrochloride, 68999-555 — Ondansetron Hydrochloride, 69339-171 — Ondansetron, 69339-172 — Ondansetron, 70518-1585 — Ondansetron Hydrochloride, 70518-3511 — Ondansetron Hydrochloride, 70518-4145 — Ondansetron Hydrochloride, 70518-4245 — Ondansetron, 71205-744 — Ondansetron Hydrochloride, 71335-0132 — Ondansetron, 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, +154 more

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