ONDANSETRON

NDC 55111-154 · Dr. Reddy's Laboratories Limited

Generic nameONDANSETRON HYDROCHLORIDE

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ONDANSETRON HYDROCHLORIDE

Strength8 mg/1

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

Marketing categoryANDA

Packages

55111-154-01 — 100 TABLET, FILM COATED in 1 BOTTLE (55111-154-01)

55111-154-05 — 500 TABLET, FILM COATED in 1 BOTTLE (55111-154-05)

55111-154-13 — 3 DOSE PACK in 1 BOX (55111-154-13) / 1 TABLET, FILM COATED in 1 DOSE PACK

55111-154-30 — 30 TABLET, FILM COATED in 1 BOTTLE (55111-154-30)

55111-154-78 — 10 DOSE PACK in 1 BOX (55111-154-78) / 10 TABLET, FILM COATED in 1 DOSE PACK (55111-154-79)

Billed under HCPCS

Q0162 — Ondansetron 1 mg, oral, fda approved prescription anti-emetic, for use as a complete therapeutic substitute for an iv anti-emetic at the time of chemotherapy treatment, not to exceed a 48 hour dosage regimen Medicare Part B payment limit (ASP + 6%): $0.02

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-933 — Ondansetron Hydrochloride, 51662-1245 — ONDANSETRON, 51662-1366 — ONDANSETRON, 51662-1377 — ONDANSETRON, 51662-1469 — ONDANSETRON, 51662-1539 — ONDANSETRON, 51662-1678 — ONDANSETRON, 54348-819 — ONDANSETRON, 54348-821 — Ondansetron Hydrochloride, 55111-153 — ONDANSETRON HYDROCHLORIDE, 55111-155 — ondansetron hydrochloride, 55111-156 — ONDANSETRON HYDROCHLORIDE, 55150-125 — Ondansetron Hydrochloride, 55150-126 — Ondansetron Hydrochloride, 55154-2876 — Ondansetron, 55154-2877 — Ondansetron, 55154-3551 — ondansetron hydrochloride, 55154-4453 — ONDANSETRON HYDROCHLORIDE, 55154-6976 — ONDANSETRON, 55154-7879 — ondansetron hydrochloride, +154 more

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