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Ondansetron

NDC 65862-391 · Aurobindo Pharma Limited

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

65862-391-01 — 1 BLISTER PACK in 1 CARTON (65862-391-01) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

65862-391-02 — 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-391-02)

65862-391-05 — 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-391-05)

65862-391-10 — 3 BLISTER PACK in 1 CARTON (65862-391-10) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

65862-391-30 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-391-30)

65862-391-66 — 6000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-391-66)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62756-356 — ondansetron, 63187-199 — Ondansetron, 63187-256 — Ondansetron, 63187-266 — Ondansetron, 63187-379 — Ondansetron, 63187-526 — Ondansetron, 63187-670 — ONDANSETRON, 63187-693 — ONDANSETRON, 63629-4306 — ONDANSETRON, 65862-390 — Ondansetron, 68001-246 — Ondansetron, 68001-247 — Ondansetron, 68071-1730 — Ondansetron, 68071-2284 — ondansetron, 68071-2718 — Ondansetron, 68071-2763 — Ondansetron, 68071-2901 — Ondansetron, 68071-3268 — Ondansetron, 68071-3926 — Ondansetron, 68071-4115 — 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.