Oxaliplatin

NDC 67184-0509 · Qilu Pharmaceutical Co., Ltd.

Generic nameoxaliplatin

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)OXALIPLATIN

Strength100 mg/20mL

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

Marketing categoryANDA

Packages

67184-0509-1 — 1 VIAL, SINGLE-USE in 1 CARTON (67184-0509-1) / 20 mL in 1 VIAL, SINGLE-USE

FDA lists these products with the same active ingredient.

43066-014 — Oxaliplatin, 43066-018 — Oxaliplatin, 55150-331 — Oxaliplatin, 55150-332 — Oxaliplatin, 60505-6132 — oxaliplatin, 60505-6287 — oxaliplatin, 61703-363 — OXALIPLATIN, 67184-0501 — Oxaliplatin, 67184-0502 — Oxaliplatin, 67184-0508 — 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, +21 more

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