Potassium Chloride Tablet, Extended Release
Product Images NDC 51655-568

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 51655-568). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 568 52 Master Bottle Label Approval Rev A 01 21)

Label (51655 568 52 Master Bottle Label Approval   Rev A 01 21)
Potassium Chloride Extended-Release Tablets USP label with 20 mEq potassium strength shown. The label states the package contains 30 tablets and is marked Rx Only. It includes storage instructions, manufacturer Northwind Health Company, LLC, and barcode information. Dosage form is extended-release tablets for oral use.*

* 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.