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Ondansetron

NDC 86211-115 · JVET PHARMACEUTICALS LLC

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

86211-115-01 — 1 VIAL in 1 CARTON (86211-115-01) / 20 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76420-917 — Ondansetron Hydrochloride, 80425-0072 — Ondansetron HCL, 80425-0074 — Ondansetron HCL, 80425-0075 — Ondansetron HCL, 82804-257 — Ondansetron Hydrochloride, 83008-074 — Ondansetron Hydrochloride, 83270-160 — ondansetron hydrochloride, 83270-161 — ondansetron hydrochloride, 83980-017 — ondansetron hydrochloride, 83980-018 — ondansetron hydrochloride, 84549-130 — ONDANSETRON, 85509-1057 — Ondansetron Hydrochloride, 85509-1075 — Ondansetron Hydrochloride, 85509-1076 — Ondansetron Hydrochloride, 85766-006 — Ondansetron Hydrochloride, 85766-053 — Ondansetron Hydrochloride, 85766-199 — ONDANSETRON, 85766-234 — ONDANSETRON, 87441-064 — Ondansetron Hydrochloride, 87441-088 — 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.