bumetanide 2 mg
INDICATIONS AND USAGE Bumetanide tablets 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 following instances of allergic reactions to furosemide suggests a lack of cross-sensitivity.
upsher-smith laboratories, llc
ROUND RED U S 42 2
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upsher-smith laboratories, llc
bumetanide 2 mg
upsher-smith laboratories, llc
bumetanide 2 mg
upsher-smith laboratories, llc
bumetanide 2 mg
upsher-smith laboratories, llc
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HOW SUPPLIED
BUMEtanIDE Tablets, USP, for oral administration, are available as:
BUMEtanIDE Tablets, USP, 0.5 mg are available as light green, round tablets with functional scoring; one side scored and debossed "U-S" above the score and "40" below the score, and the other side unscored and debossed "0.5". Tablets are supplied as: NDC 0832-0540-11 bottles of 100
BUMEtanIDE Tablets, USP, 1 mg are available as yellow, round tablets with functional scoring; one side scored and debossed "U-S" above the score and "41" below the score, and the other side unscored and debossed "1". Tablets are supplied as: NDC 0832-0541-11 bottles of 100 NDC 0832-0541-10 bottles of 1000
BUMEtanIDE Tablets, USP , 2 mg are available as light red, round tablets with functional scoring; one side scored and debossed "U-S" above the score and "42" below the score, and the other side unscored and debossed "2". Tablets are supplied as: NDC 0832-0542-11 bottles of 100 NDC 0832-0542-10 bottles of 1000 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.
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