potassium chloride tablet extended release
INDICATIONS AND USAGE BECAUSE OF REPORTS OF INTESTINAL AND GASTRIC ULCERATION AND BLEEDING WITH CONTROLLED-RELEASE POTASSIUM CHLORIDE PREPARATIONS, THESE DRUGS SHOULD BE RESERVED FOR THOSE PATIENTS WHO CANNOT TOLERATE OR REFUSE TO TAKE LIQUID OR EFFERVESCENT POTASSIUM PREPARATIONS OR FOR PATIENTS IN WHOM THERE IS A PROBLEM OF COMPLIANCE WITH THESE PREPARATIONS. For the treatment of patients with hypokalemia with or without metabolic alkalosis, in digitalis intoxication, and in patients with hypokalemic familial periodic paralysis. If hypokalemia is the result of diuretic therapy, consideration should be given to the use of a lower dose of diuretic, which may be sufficient without leading to hypokalemia. For the prevention of hypokalemia in patients who would be at particular risk if hypokalemia were to develop, e.g., digitalized patients or patients with significant cardiac arrhythmias. The use of potassium salts in patients receiving diuretics for uncomplicated essential hypertension is often unnecessary when such patients have a normal dietary pattern and when low doses of the diuretic are used. Serum potassium should be checked periodically, however, and if hypokalemia occurs, dietary supplementation with potassium-containing foods may be adequate to control milder cases. In more severe cases, and if dose adjustment of the diuretic is ineffective or unwarranted, supplementation with potassium salts may be indicated.
cadila healthcare limited
OVAL WHITE KCI10
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potassium chloride tablet extended release
cadila healthcare limited
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HOW SUPPLIED
POTASSIUM CHLORIDE Extended-release Tablets, USP 10 mEq are white to off-white colored, capsule shaped, biconvex uncoated tablets debossed with "KCl 10" on one side and plain on the other side and are supplied as follows: NDC 70771-1599-1 in bottle of 100 tablets NDC 70771-1599-0 in bottle of 1000 tablets
POTASSIUM CHLORIDE Extended-release Tablets, USP 20 mEq are white to off-white colored, capsule shaped, biconvex uncoated tablets debossed with "KCl" and "20" on either side of break line and plain on the other side and are supplied as follows: NDC 70771-1600-1 in bottle of 100 tablets NDC 70771-1600-5 in bottle of 500 tablets NDC 70771-1600-0 in bottle of 1000 tablets Keep tightly closed. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
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