Potassium Chloride Tablet, Extended Release
Product Images NDC 24979-232

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 24979-232). 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.

Product Images & Figures Index

FDA Label Image

Principal Display Panel (750 mg Tablet Bottle Label)

Principal Display Panel (750 mg Tablet Bottle Label)
Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq) oral tablet packaging label by Upsher-Smith Laboratories, LLC. The label indicates 100 film-coated tablets, prescription use, with storage instructions and manufacturer information. The NDC is 24979-231-01.*
FDA Label Image

Principal Display Panel (750 mg Tablet Bottle Label)

Principal Display Panel (750 mg Tablet Bottle Label)
Label for Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq) oral film-coated tablets. The package contains 500 tablets and is labeled for prescription use only. It is manufactured for TWi Pharmaceuticals USA, Inc. and by Bora Pharmaceutical Laboratories Inc. The label includes storage instructions at 20°C to 25°C and a warning not to accept if the safety seal is broken or missing.*
FDA Label Image

Principal Display Panel (1500 mg Tablet Bottle Label)

Principal Display Panel (1500 mg Tablet Bottle Label)
Label for Potassium Chloride Extended-Release Tablets, USP 20 mEq (1500 mg), oral extended-release film-coated tablets. The package contains 100 tablets. The label includes storage instructions, manufacturing details for TWi Pharmaceuticals USA and Bora Pharmaceutical Laboratories, and a caution regarding the seal over the bottle opening. The NDC number 24979-232-01 is shown with a barcode.*

* 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.