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Ondansetron

NDC 65162-691 · Amneal Pharmaceuticals LLC

Generic nameOndansetron
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength4 mg/5mL
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

65162-691-19 — 10 CUP, UNIT-DOSE in 1 TRAY (65162-691-19) / 5 mL in 1 CUP, UNIT-DOSE (65162-691-37)

65162-691-79 — 50 mL in 1 BOTTLE (65162-691-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-236 — ONDANSETRON, 63187-513 — ondansetron hydrochloride, 63187-636 — Ondansetron Hydrochloride, 63187-709 — Ondansetron Hydrochloride, 63304-458 — ONDANSETRON, 63304-459 — ONDANSETRON, 63323-373 — ONDANSETRON HYDROCHLORIDE, 63323-374 — ONDANSETRON HYDROCHLORIDE, 63850-0003 — Ondansetron Tablets, 63850-0004 — Ondansetron Tablets, 65219-323 — ONDANSETRON HYDROCHLORIDE, 65862-187 — Ondansetron Hydrochloride, 65862-188 — Ondansetron Hydrochloride, 65862-189 — Ondansetron Hydrochloride, 65862-208 — Ondansetron Hydrochloride, 67046-1242 — Ondansetron Hydrochloride, 67184-0507 — ONDANSETRON, 67296-1562 — Ondansetron Hydrochloride, 67296-2119 — Ondansetron, 67877-170 — Ondansetron Hydrochloride, +154 more

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