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ONDANSETRON

NDC 51662-1469 · HF Acquisition Co LLC, DBA HealthFirst

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

Packages

51662-1469-1 — 2 mL in 1 VIAL, SINGLE-DOSE (51662-1469-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 51662-1245 — ONDANSETRON, 51662-1366 — ONDANSETRON, 51662-1377 — ONDANSETRON, 51662-1539 — ONDANSETRON, 51662-1678 — ONDANSETRON, 54348-819 — ONDANSETRON, 54348-821 — Ondansetron Hydrochloride, 55111-153 — ONDANSETRON HYDROCHLORIDE, 55111-154 — ONDANSETRON HYDROCHLORIDE, 55111-155 — ondansetron hydrochloride, 55111-156 — ONDANSETRON HYDROCHLORIDE, 55150-125 — Ondansetron Hydrochloride, 55150-126 — 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.