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ONDANSETRON

NDC 62135-351 · Chartwell RX, LLC

Generic nameONDANSETRON
Dosage formTABLET
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength8 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

62135-351-05 — 500 TABLET in 1 BOTTLE (62135-351-05)

62135-351-30 — 30 TABLET in 1 BOTTLE (62135-351-30)

Billed under HCPCS

Q0162 — Ondansetron 1 mg, oral, fda approved prescription anti-emetic, for use as a complete therapeutic substitute for an iv anti-emetic at the time of chemotherapy treatment, not to exceed a 48 hour dosage regimen Medicare Part B payment limit (ASP + 6%): $0.02

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 61919-565 — ONDANSETRON, 62135-350 — 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, 63304-458 — ONDANSETRON, 63304-459 — ONDANSETRON, +154 more