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FDA (Drug enforcement)Recalled 2024-05-30class i

Glenmark Pharmaceuticals Inc., USA: Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot No. 2, Phase-2,

Hazard

Failed Dissolution Specifications

Details from the source

Reason for recall: Failed Dissolution Specifications Distribution: Nationwide Quantity: 285,840 bottles Lot/code info: Lot#: 17221446, 17221445, Exp May-31-24; 17221393, 17221403, 17221405, 17221503, 17221508, Exp Jun-30-24; 17221567, 17221566, 17221719, 17221731, Exp Jul-31-24; 17221891, 17221892, 17221900, 17221992, 17222022, Exp Aug-31-24; 17222056, 17222043, 17222068, 17222079, 17222099, 17222103, 17222114, 17222119, 17222188, 17222199, 17222209, 17222200, Exp Sep-30-24; 17222265, 17222269, Exp Oct-31-24; 17222527, 17222530, 17222583, 17222586, 17230051, 17230075, 17230067, Exp Nov-30-24;

Source

Official record: FDA (Drug enforcement)

Republished from the official source above; details can change — the source record controls.

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