Bumetanide
NDC 51672-4225 · Sun Pharmaceutical Industries, Inc.
Packages
51672-4225-1 — 100 TABLET in 1 BOTTLE (51672-4225-1)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
50090-7736 — Bumetanide, 50090-7854 — Bumetanide, 50090-7876 — Bumetanide, 50090-7965 — Bumetanide, 50268-130 — Bumetanide, 50268-131 — Bumetanide, 50268-132 — Bumetanide, 51662-1449 — BUMETANIDE, 51672-4223 — Bumetanide, 51672-4224 — Bumetanide, 55154-1527 — Bumetanide, 55154-3572 — Bumetanide, 55154-4345 — Bumetanide, 55154-5131 — Bumetanide, 60687-384 — Bumetanide, 60687-535 — Bumetanide, 63629-4968 — Bumetanide, 65219-570 — Bumetanide, 65219-572 — Bumetanide, 67184-0593 — Bumetanide, +105 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.
T50.1X1 — Poisoning by loop [high-ceiling] diuretics, accidental (unintentional), T50.1X2 — Poisoning by loop [high-ceiling] diuretics, intentional self-harm, T50.1X3 — Poisoning by loop [high-ceiling] diuretics, assault, T50.1X4 — Poisoning by loop [high-ceiling] diuretics, undetermined, T50.1X5 — Adverse effect of loop [high-ceiling] diuretics, T50.1X6 — Underdosing of loop [high-ceiling] diuretics