Potassium Chloride Tablet, Film Coated, Extended Release
Product Images NDC 0832-5322

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 0832-5322). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, 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 (600 mg Tablet Bottle Label)

Potassium Chloride Extended-Release Tablets, USP 600 mg (8 mEq), film-coated and oral dosage form, in a 100-tablet package. The label indicates it is a prescription drug by Upsher-Smith Laboratories, LLC. Storage and dosage instructions are included along with the barcode and manufacturer details.*

FDA Label Image

Principal Display Panel (750 mg Tablet Bottle Label)

Label for Potassium Chloride Extended-Release Tablets, USP, 750 mg (10 mEq), in a package of 100 tablets. The label includes storage instructions, usage cautions, and manufacturer information for Upsher-Smith Laboratories, LLC, Maple Grove, MN.*

* 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.