Ondansetron

NDC 51407-004 · Golden State Medical Supply, Inc.

Generic nameOndansetron

Dosage formTABLET

RouteORAL

Active ingredient(s)ONDANSETRON HYDROCHLORIDE

Strength8 mg/1

Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

Marketing categoryANDA

Packages

51407-004-05 — 500 TABLET in 1 BOTTLE (51407-004-05)

51407-004-30 — 30 TABLET in 1 BOTTLE (51407-004-30)

FDA lists these products with the same active ingredient.

43063-792 — Ondansetron Hydrochloride, 50090-3178 — Ondansetron Hydrochloride, 50090-3185 — Ondansetron Hydrochloride, 50090-4671 — Ondansetron Hydrochloride, 50090-4935 — ONDANSETRON, 50090-6342 — Ondansetron Hydrochloride, 50268-621 — Ondansetron Hydrochloride, 50268-622 — Ondansetron Hydrochloride, 50268-647 — Ondansetron, 51407-003 — Ondansetron, 51655-016 — Ondansetron Hydrochloride, 51655-415 — Ondansetron Hydrochloride, 51655-813 — Ondansetron Hydrochloride, 51655-933 — Ondansetron Hydrochloride, 51662-1245 — ONDANSETRON, 51662-1366 — ONDANSETRON, 51662-1377 — ONDANSETRON, 51662-1469 — ONDANSETRON, 51662-1539 — ONDANSETRON, 51662-1678 — ONDANSETRON, +154 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.