Skip to main content

Ondansetron

NDC 17856-0672 · Atlantic Biologics Corp.

Generic nameOndansetron Hydrochloride
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

17856-0672-1 — 60 SYRINGE in 1 CASE (17856-0672-1) / 2.5 mL in 1 SYRINGE

17856-0672-2 — 120 SYRINGE in 1 CASE (17856-0672-2) / 2.5 mL in 1 SYRINGE

17856-0672-3 — 120 SYRINGE in 1 CASE (17856-0672-3) / 2.5 mL in 1 SYRINGE

17856-0672-4 — 72 CUP, UNIT-DOSE in 1 CASE (17856-0672-4) / 5 mL in 1 CUP, UNIT-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8185 — ondansetron hydrochloride, 0641-6078 — Ondansetron, 0641-6079 — Ondansetron, 0641-6080 — Ondansetron, 0641-6286 — Ondansetron, 0904-6551 — ondansetron hydrochloride, 0904-6552 — ondansetron hydrochloride, 16714-159 — Ondansetron, 16714-160 — Ondansetron, 16714-671 — Ondansetron Hydrochloride, 17856-0691 — Ondansetron, 23155-547 — ONDANSETRON, 23155-548 — ONDANSETRON, 23155-549 — ONDANSETRON, 23155-550 — ONDANSETRON, 25021-777 — ondansetron hydrochloride, 36000-012 — ONDANSETRON HYDROCHLORIDE, 42708-044 — Ondansetron Hydrochloride, 42708-059 — Ondansetron Hydrochloride, 42708-179 — 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.