Allopurinol

NDC 65219-380 · Fresenius Kabi USA, LLC

Generic nameAllopurinol

Dosage formINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

RouteINTRAVENOUS

Active ingredient(s)ALLOPURINOL SODIUM

Strength500 mg/25mL

Pharmacologic classXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]

Marketing categoryANDA

Packages

65219-380-30 — 1 VIAL, GLASS in 1 CARTON (65219-380-30) / 25 mL in 1 VIAL, GLASS

Billed under HCPCS

J0206 — Injection, allopurinol sodium, 1 mg Medicare Part B payment limit (ASP + 6%): $4.07

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9533 — Allopurinol sodium, 67457-187 — Allopurinol, 68083-380 — Allopurinol

Poisoning, adverse-effect and underdosing codes for this drug

The ICD-10-CM Table of Drugs and Chemicals carries these diagnosis codes for this drug — a drug-name match derived from FDA's product name and the Table of Drugs and Chemicals, not a CMS-published pairing.

T50.4X1 — Poisoning by drugs affecting uric acid metabolism, accidental (unintentional), T50.4X2 — Poisoning by drugs affecting uric acid metabolism, intentional self-harm, T50.4X3 — Poisoning by drugs affecting uric acid metabolism, assault, T50.4X4 — Poisoning by drugs affecting uric acid metabolism, undetermined, T50.4X5 — Adverse effect of drugs affecting uric acid metabolism, T50.4X6 — Underdosing of drugs affecting uric acid metabolism

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