Oxaliplatin

NDC 68083-170 · Gland Pharma Limited

Generic nameOxaliplatin

Dosage formINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

RouteINTRAVENOUS

Active ingredient(s)OXALIPLATIN

Strength50 mg/10mL

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

Marketing categoryANDA

Packages

68083-170-01 — 10 mL in 1 VIAL (68083-170-01)

FDA lists these products with the same active ingredient.

60505-6287 — oxaliplatin, 61703-363 — OXALIPLATIN, 67184-0501 — Oxaliplatin, 67184-0502 — Oxaliplatin, 67184-0508 — oxaliplatin, 67184-0509 — oxaliplatin, 67184-0510 — Oxaliplatin, 67457-442 — Oxaliplatin, 67457-469 — Oxaliplatin, 68001-468 — Oxaliplatin, 68083-171 — Oxaliplatin, 68083-176 — Oxaliplatin, 68083-177 — Oxaliplatin, 68083-314 — Oxaliplatin, 71288-101 — Oxaliplatin, 71288-149 — Oxaliplatin, 71288-171 — Oxaliplatin, 71288-172 — Oxaliplatin, 72266-161 — Oxaliplatin, 72266-162 — 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.