Potassium Chloride Tablet, Film Coated, Extended Release
Product Images NDC 68001-518

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 68001-518). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

100 Tablet Label (Potassium Fig3)

This label panel for Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq) includes the National Drug Code 68001-518-00 and specifies 100 tablets per container. It provides dosing, storage instructions, and patient information. The label mentions the manufacturer, APL Healthcare Limited in India, and BluePoint Laboratories as the labeler. The extended-release feature and caution about the matrix not being absorbed are noted.*

* 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.