Bumetanide 1 mg
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 tablets, USP following instances of allergic reactions to furosemide suggests a lack of cross-sensitivity.
Eon Labs, Inc.
ROUND YELLOW E 129
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Bumetanide 1 mg
Eon Labs, Inc.
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HOW SUPPLIED
BUMEtanIDE Tablets, USP, for oral administration, are available as 0.5 mg green, round, biconvex, bisected and debossed “E” above and “128” below the bisect on one side and plain on the reverse side and supplied as: NDC 0185-0128-01 bottles of 100 NDC 0185-0128-05 bottles of 500 1 mg yellow, round, biconvex, bisected and debossed “E” above and “129” below the bisect on one side and plain on the reverse side and supplied as: NDC 0185-0129-01 bottles of 100 NDC 0185-0129-05 bottles of 500 2 mg beige to light brown, round, biconvex, bisected and debossed “E” above and “130” below the bisect on one side and plain on the reverse side and supplied as: NDC 0185-0130-01 bottles of 100 NDC 0185-0130-05 bottles of 500 Storage Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Dispense contents in a tight, light-resistant container as defined in the USP with a child-resistant closure, as required. KEEP TIGHTLY CLOSED. Manufactured in India by Sandoz Private Ltd., for Sandoz Inc., Princeton, NJ 08540 Rev. Jun 2023 46326538
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