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ONDANSETRON

NDC 51662-1678 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameONDANSETRON
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength4 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

51662-1678-1 — 30 TABLET, FILM COATED in 1 BOTTLE (51662-1678-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-004 — 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, 54348-819 — ONDANSETRON, 54348-821 — Ondansetron Hydrochloride, 55111-153 — ONDANSETRON HYDROCHLORIDE, 55111-154 — ONDANSETRON HYDROCHLORIDE, 55111-155 — ondansetron hydrochloride, 55111-156 — ONDANSETRON HYDROCHLORIDE, 55150-125 — Ondansetron Hydrochloride, 55150-126 — Ondansetron Hydrochloride, 55154-2876 — Ondansetron, 55154-2877 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels