Allopurinol
NDC 70518-3660 · REMEDYREPACK INC.
Packages
70518-3660-0 — 30 TABLET in 1 BLISTER PACK (70518-3660-0)
70518-3660-2 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-3660-2)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
68788-8337 — Allopurinol, 68788-8364 — Allopurinol, 68788-8424 — allopurinol, 68788-8458 — Allopurinol, 68788-8713 — Allopurinol, 68788-8727 — Allopurinol, 68788-8865 — ALLOPURINOL, 69315-291 — Allopurinol, 69315-292 — Allopurinol, 69315-409 — Allopurinol, 70518-3704 — Allopurinol, 70518-4062 — Allopurinol, 70518-4286 — allopurinol, 70518-4404 — ALLOPURINOL, 70518-4412 — allopurinol, 70518-4556 — Allopurinol, 70518-4693 — Allopurinol, 70710-1209 — Allopurinol, 70710-1210 — Allopurinol, 70710-2009 — Allopurinol, +142 more
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