Allopurinol
NDC 68071-3605 · NuCare Pharmaceuticals,Inc.
Packages
68071-3605-9 — 90 TABLET in 1 BOTTLE (68071-3605-9)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
63629-2113 — allopurinol, 66267-665 — allopurinol, 67046-0681 — Allopurinol, 67046-1514 — allopurinol, 67046-1639 — Allopurinol, 67046-1658 — Allopurinol, 67296-1897 — Allopurinol, 67544-313 — Allopurinol, 67544-736 — allopurinol, 68071-2997 — Allopurinol, 68071-3672 — Allopurinol, 68071-3803 — Allopurinol, 68071-3871 — Allopurinol, 68788-4027 — ALLOPURINOL, 68788-6323 — ALLOPURINOL, 68788-8337 — Allopurinol, 68788-8364 — Allopurinol, 68788-8424 — allopurinol, 68788-8458 — Allopurinol, 68788-8713 — 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