Allopurinol
NDC 62135-517 · Chartwell RX, LLC
Packages
62135-517-31 — 300 TABLET in 1 BOTTLE (62135-517-31)
62135-517-90 — 90 TABLET in 1 BOTTLE (62135-517-90)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
55154-7981 — allopurinol, 59651-285 — Allopurinol, 59651-286 — Allopurinol, 60687-677 — Allopurinol, 60687-688 — Allopurinol, 60760-656 — Allopurinol, 60760-710 — Allopurinol, 60760-722 — Allopurinol, 60760-989 — Allopurinol, 62135-516 — Allopurinol, 63187-240 — Allopurinol, 63187-463 — Allopurinol, 63629-1781 — Allopurinol, 63629-2111 — allopurinol, 63629-2112 — allopurinol, 63629-2113 — allopurinol, 66267-665 — allopurinol, 67046-0681 — Allopurinol, 67046-1514 — allopurinol, 67046-1639 — 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