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ONDANSETRON

NDC 50090-4935 · A-S Medication Solutions

Generic nameONDANSETRON
Dosage formINJECTION
RouteINTRAMUSCULAR, INTRAVENOUS
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength2 mg/mL
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

50090-4935-0 — 25 VIAL, SINGLE-USE in 1 CARTON (50090-4935-0) / 2 mL in 1 VIAL, SINGLE-USE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

25021-777 — ondansetron hydrochloride, 36000-012 — ONDANSETRON HYDROCHLORIDE, 42708-044 — Ondansetron Hydrochloride, 42708-059 — Ondansetron Hydrochloride, 42708-179 — Ondansetron Hydrochloride, 43063-770 — Ondansetron, 43063-792 — Ondansetron Hydrochloride, 50090-3178 — Ondansetron Hydrochloride, 50090-3185 — Ondansetron Hydrochloride, 50090-4671 — Ondansetron Hydrochloride, 50090-6342 — Ondansetron Hydrochloride, 50268-621 — Ondansetron Hydrochloride, 50268-622 — Ondansetron Hydrochloride, 50268-647 — Ondansetron, 51407-003 — Ondansetron, 51407-004 — Ondansetron, 51655-016 — Ondansetron Hydrochloride, 51655-415 — Ondansetron Hydrochloride, 51655-813 — Ondansetron Hydrochloride, 51655-933 — 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.