NDC 68382-0526-05

bumetanide 1 mg/1 TABLET

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NDC

68382-0526-05

Generic Name

bumetanide

Brand Name

bumetanide

Strength

1 mg/1

Dosage Form

TABLET

Route

ORAL

Package Size

—

Labeler

Zydus Pharmaceuticals (USA) Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Bumetanide tablets USP are indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including the nephrotic syndrome. Almost equal diuretic response occurs after oral and parenteral administration of bumetanide. Therefore, if impaired gastrointestinal absorption is suspected or oral administration is not practical, bumetanide should be given by the intramuscular or intravenous route. Successful treatment with bumetanide table…

Important Warnings

WARNINGS Volume and Electrolyte Depletion The dose of bumetanide should be adjusted to the patient’s need. Excessive doses or too frequent administration can lead to profound water loss, electrolyte depletion, dehydration, reduction in blood volume and circulatory collapse with the possibility of vascular thrombosis and embolism, particularly in elderly patients. Hypokalemia Hypokalemia can occur…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other bumetanide NDC Codes

42799-0119-01.5 mg/1TABLET

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