Allopurinol
NDC 71921-242 · Florida Pharmaceutical Products, LLC
Packages
71921-242-01 — 100 TABLET in 1 BOTTLE (71921-242-01)
71921-242-50 — 500 TABLET in 1 BOTTLE (71921-242-50)
71921-242-60 — 1000 TABLET in 1 BOTTLE (71921-242-60)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
71610-064 — Allopurinol, 71610-194 — Allopurinol, 71610-197 — Allopurinol, 71610-253 — Allopurinol, 71610-676 — Allopurinol, 71610-678 — allopurinol, 71610-681 — Allopurinol, 71610-949 — Allopurinol, 71921-240 — Allopurinol, 71921-241 — Allopurinol, 72162-1149 — allopurinol, 72162-1150 — allopurinol, 72189-417 — ALLOPURINOL, 72189-437 — Allopurinol, 72189-647 — Allopurinol, 72865-303 — ALLOPURINOL, 72865-304 — ALLOPURINOL, 80425-0206 — Allopurinol, 80425-0383 — allopurinol, 80425-0518 — 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