Allopurinol
NDC 70771-1907 · Zydus Lifesciences Limited
Packages
70771-1907-0 — 1000 TABLET in 1 BOTTLE (70771-1907-0)
70771-1907-9 — 90 TABLET in 1 BOTTLE (70771-1907-9)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
70518-4286 — allopurinol, 70518-4404 — ALLOPURINOL, 70518-4412 — allopurinol, 70518-4556 — Allopurinol, 70518-4693 — Allopurinol, 70710-1209 — Allopurinol, 70710-1210 — Allopurinol, 70710-2009 — Allopurinol, 70771-1126 — Allopurinol, 70771-1127 — Allopurinol, 71205-049 — ALLOPURINOL, 71205-208 — Allopurinol, 71205-377 — Allopurinol, 71335-0112 — ALLOPURINOL, 71335-0467 — allopurinol, 71335-1656 — allopurinol, 71335-2332 — Allopurinol, 71335-2347 — Allopurinol, 71335-2416 — Allopurinol, 71335-2542 — 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