Potassium Chloride Tablet, Extended Release
Product Images NDC 0832-5324

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 0832-5324). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smithlaboratories, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Principal Display Panel (10 mEq K Tablet Bottle Label)

Label for Potassium Chloride Extended-Release Tablets USP, 750 mg strength, providing 10 mEq potassium per tablet. The label indicates a package of 100 tablets, extended-release oral dosage form, manufactured by Upsher-Smith Laboratories, LLC. Includes storage instructions, prescribing notes, barcode, and trademark information.*

FDA Label Image

Principal Display Panel (20 mEq K Tablet Bottle Label)

Label for Potassium Chloride Extended-Release Tablets, USP, 20 mEq strength, micro-dispersible technology. The label states the dosage form as extended-release tablets and notes 100 tablets per container. Manufactured by Upsher-Smith Laboratories, LLC, Maple Grove, MN. Usage and storage instructions, bar code, and trademark information are included.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.