ONDANSETRON

NDC 63187-065 · Proficient Rx LP

Generic nameONDANSETRON

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

63187-065-10 — 10 TABLET, FILM COATED in 1 BOTTLE (63187-065-10)

63187-065-15 — 15 TABLET, FILM COATED in 1 BOTTLE (63187-065-15)

63187-065-20 — 20 TABLET, FILM COATED in 1 BOTTLE (63187-065-20)

63187-065-30 — 30 TABLET, FILM COATED in 1 BOTTLE (63187-065-30)

63187-065-60 — 60 TABLET, FILM COATED in 1 BOTTLE (63187-065-60)

63187-065-90 — 90 TABLET, FILM COATED in 1 BOTTLE (63187-065-90)

FDA lists these products with the same active ingredient.

60687-252 — Ondansetron, 60760-636 — Ondansetron Hydrochloride, 60760-658 — Ondansetron Hydrochloride, 60760-878 — Ondansetron Hydrochloride, 61919-565 — ONDANSETRON, 62135-350 — ONDANSETRON, 62135-351 — ONDANSETRON, 62135-555 — Ondansetron Hydrochloride, 62756-130 — ondansetron hydrochloride, 62756-131 — ondansetron hydrochloride, 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, +154 more

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