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Ondansetron Hydrochloride

NDC 65862-189 · Aurobindo Pharma Limited

Generic nameOndansetron Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength24 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

65862-189-11 — 1 BLISTER PACK in 1 CARTON (65862-189-11) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63304-458 — ONDANSETRON, 63304-459 — ONDANSETRON, 63323-373 — ONDANSETRON HYDROCHLORIDE, 63323-374 — ONDANSETRON HYDROCHLORIDE, 63850-0003 — Ondansetron Tablets, 63850-0004 — Ondansetron Tablets, 65162-691 — Ondansetron, 65219-323 — ONDANSETRON HYDROCHLORIDE, 65862-187 — Ondansetron Hydrochloride, 65862-188 — Ondansetron Hydrochloride, 65862-208 — Ondansetron Hydrochloride, 67046-1242 — Ondansetron Hydrochloride, 67184-0507 — ONDANSETRON, 67296-1562 — Ondansetron Hydrochloride, 67296-2119 — Ondansetron, 67877-170 — Ondansetron Hydrochloride, 68071-1742 — Ondansetron Hydrochloride, 68071-2053 — Ondansetron Hydrochloride, 68071-3611 — Ondansetron Hydrochloride, 68071-3713 — 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.