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NDC 68462-0472-01

potassium chloride 1500 mg/1 TABLET, EXTENDED RELEASE

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NDC
68462-0472-01
Generic Name
potassium chloride
Brand Name
potassium chloride
Strength
1500 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Package Size
Labeler
Glenmark Pharmaceuticals Inc., USA

FDA Drug Information

Indications & Usage

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. 1. For the treatment of patients with hypokalemia with or without metabolic alkalosis, in digitalis intoxication, and in patients with h…

Important Warnings

WARNINGS Hyperkalemia (see OVERDOSAGE ) In patients with impaired mechanisms for excreting potassium, the administration of potassium salts can produce hyperkalemia and cardiac arrest. This occurs most commonly in patients given potassium by the intravenous route but may also occur in patients given potassium orally. Potentially fatal hyperkalemia can develop rapidly and be asymptomatic. The use o…

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

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