Oxaliplatin

NDC 71288-171 · Meitheal Pharmaceuticals Inc.

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameOxaliplatin

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)OXALIPLATIN

Strength5 mg/mL

Pharmacologic classPlatinum-based Drug [EPC], Platinum-containing Compounds [EXT]

Marketing categoryANDA

Packages

71288-171-11 — 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-171-11) / 10 mL in 1 VIAL, SINGLE-DOSE

71288-171-91 — 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-171-91) / 10 mL in 1 VIAL, SINGLE-DOSE

J9263 — Injection, oxaliplatin, 0.5 mg Medicare Part B payment limit (ASP + 6%): $0.06

FDA lists these products with the same active ingredient.

67184-0508 — oxaliplatin, 67184-0509 — oxaliplatin, 67184-0510 — Oxaliplatin, 67457-442 — Oxaliplatin, 67457-469 — Oxaliplatin, 68001-468 — Oxaliplatin, 68083-170 — Oxaliplatin, 68083-171 — Oxaliplatin, 68083-176 — Oxaliplatin, 68083-177 — Oxaliplatin, 68083-314 — Oxaliplatin, 71288-101 — Oxaliplatin, 71288-149 — Oxaliplatin, 71288-172 — Oxaliplatin, 72266-161 — Oxaliplatin, 72266-162 — Oxaliplatin, 72603-101 — Oxaliplatin, 72603-301 — Oxaliplatin, 72603-320 — Oxaliplatin, 72603-420 — Oxaliplatin, +21 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.