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Ondansetron

NDC 70518-1551 · REMEDYREPACK INC.

Generic nameOndansetron
Dosage formTABLET, ORALLY DISINTEGRATING
RouteORAL
Active ingredient(s)ONDANSETRON
Strength8 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

70518-1551-0 — 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (70518-1551-0)

70518-1551-1 — 3 BLISTER PACK in 1 CARTON (70518-1551-1) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-5021 — Ondansetron, 68071-5167 — Ondansetron, 68071-5230 — ondansetron, 68462-157 — Ondansetron, 68462-158 — Ondansetron, 68788-4133 — Ondansetron, 68788-7565 — Ondansetron, 68788-7644 — Ondansetron, 68788-8666 — Ondansetron, 68788-9559 — Ondansetron, 70518-3512 — Ondansetron, 70518-4685 — Ondansetron, 71205-713 — Ondansetron, 71335-0650 — Ondansetron, 71335-1071 — Ondansetron, 71335-1314 — Ondansetron, 71335-1731 — Ondansetron, 71335-2635 — Ondansetron, 71335-2972 — Ondansetron, 71335-2973 — Ondansetron, +78 more

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