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ONDANSETRON

NDC 61919-565 · Direct_Rx

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

61919-565-30 — 30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)

61919-565-45 — 45 TABLET, FILM COATED in 1 BOTTLE (61919-565-45)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-7879 — ondansetron hydrochloride, 55700-627 — Ondansetron Hydrochloride, 55700-631 — Ondansetron Hydrochloride, 57237-075 — Ondansetron Hydrochloride, 57237-076 — Ondansetron Hydrochloride, 60505-6130 — ONDANSETRON, 60687-252 — Ondansetron, 60760-636 — Ondansetron Hydrochloride, 60760-658 — Ondansetron Hydrochloride, 60760-878 — Ondansetron Hydrochloride, 62135-350 — ONDANSETRON, 62135-351 — ONDANSETRON, 62135-555 — Ondansetron Hydrochloride, 62756-130 — ondansetron hydrochloride, 62756-131 — ondansetron hydrochloride, 63187-065 — ONDANSETRON, 63187-236 — ONDANSETRON, 63187-513 — ondansetron hydrochloride, 63187-636 — Ondansetron Hydrochloride, 63187-709 — 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.