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Ondansetron

NDC 76420-251 · Asclemed USA, 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

76420-251-04 — 4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (76420-251-04)

76420-251-06 — 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (76420-251-06)

76420-251-10 — 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (76420-251-10)

76420-251-20 — 20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (76420-251-20)

76420-251-30 — 3 BLISTER PACK in 1 CARTON (76420-251-30) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1731 — Ondansetron, 71335-2635 — Ondansetron, 71335-2972 — Ondansetron, 71335-2973 — Ondansetron, 71335-2974 — Ondansetron, 71335-3073 — Ondansetron, 71335-9726 — Ondansetron, 72336-073 — Ondansetron, 76420-056 — Ondansetron, 76420-217 — Ondansetron, 80425-0073 — Ondansetron, 80425-0222 — Ondansetron, 80425-0227 — Ondansetron, 80425-0228 — Ondansetron, 80425-0469 — Ondansetron, 80425-0473 — Ondansetron, 83980-012 — Ondansetron, 83980-013 — Ondansetron, 85534-0025 — Ondansetron, 85534-0063 — 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.