Ondansetron
NDC 68462-106 · Glenmark Pharmaceuticals Inc., USA
Packages
68462-106-30 — 30 TABLET, FILM COATED in 1 BOTTLE (68462-106-30)
68462-106-33 — 1 BLISTER PACK in 1 CARTON (68462-106-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
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.
68071-4328 — Ondansetron Hydrochloride, 68071-4705 — Ondansetron Hydrochloride, 68071-4966 — Ondansetron Hydrochloride, 68071-5047 — Ondansetron Hydrochloride, 68083-113 — Ondansetron, 68083-114 — Ondansetron, 68084-220 — Ondansetron Hydrochloride, 68084-221 — Ondansetron Hydrochloride, 68094-763 — Ondansetron Hydrochloride, 68462-105 — Ondansetron, 68788-8582 — Ondansetron Hydrochloride, 68788-8651 — Ondansetron Hydrochloride, 68788-9368 — Ondansetron Hydrochloride, 68788-9402 — Ondansetron Hydrochloride, 68999-555 — Ondansetron Hydrochloride, 69339-171 — Ondansetron, 69339-172 — Ondansetron, 70518-1585 — Ondansetron Hydrochloride, 70518-3511 — Ondansetron Hydrochloride, 70518-4145 — Ondansetron Hydrochloride, +154 more