Allopurinol
NDC 51655-082 · Northwind Health Company, LLC
Packages
51655-082-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-082-52)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
50090-7351 — Allopurinol, 50090-7353 — Allopurinol, 50090-7696 — ALLOPURINOL, 50090-7697 — ALLOPURINOL, 50090-7791 — ALLOPURINOL, 50090-7792 — ALLOPURINOL, 50090-7832 — Allopurinol, 50090-7833 — Allopurinol, 51079-205 — allopurinol, 51079-206 — allopurinol, 51655-523 — allopurinol, 51655-546 — allopurinol, 51655-782 — allopurinol, 51655-945 — Allopurinol, 51655-968 — Allopurinol, 53401-019 — ALLOPURINOL, 53401-025 — ALLOPURINOL, 53489-156 — Allopurinol, 53489-157 — Allopurinol, 55111-729 — 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