Ondansetron

NDC 69339-171 · Natco Pharma USA LLC

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

69339-171-01 — 100 TABLET in 1 BOTTLE (69339-171-01)

69339-171-03 — 30 TABLET in 1 BOTTLE (69339-171-03)

69339-171-05 — 500 TABLET in 1 BOTTLE (69339-171-05)

FDA lists these products with the same active ingredient.

68084-220 — Ondansetron Hydrochloride, 68084-221 — Ondansetron Hydrochloride, 68094-763 — Ondansetron Hydrochloride, 68462-105 — Ondansetron, 68462-106 — Ondansetron, 68788-8582 — Ondansetron Hydrochloride, 68788-8651 — Ondansetron Hydrochloride, 68788-9368 — Ondansetron Hydrochloride, 68788-9402 — Ondansetron Hydrochloride, 68999-555 — Ondansetron Hydrochloride, 69339-172 — Ondansetron, 70518-1585 — Ondansetron Hydrochloride, 70518-3511 — Ondansetron Hydrochloride, 70518-4145 — Ondansetron Hydrochloride, 70518-4245 — Ondansetron, 70518-4588 — Ondansetron, 71205-744 — Ondansetron Hydrochloride, 71335-0132 — Ondansetron, 71335-0205 — Ondansetron Hydrochloride, 71335-0815 — 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.