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

Product Visual Gallery

This gallery contains 7 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.

FDA Label Image

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

Image Description (Usl 10 100)

Potassium Chloride Extended-Release Tablets, USP 10 mEq (750 mg) film-coated tablets, 100 count, labeled for oral use. The label includes directions for sealed bottle integrity, storage recommendations, dosage information, and manufacturer details: Upsher-Smith Laboratories, LLC, Maple Grove, MN.*

FDA Label Image

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

Image Description (Usl 10 500)

Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq) film-coated tablets, labeled by Upsher-Smith Laboratories, LLC. The label notes a package count of 500 tablets and includes storage instructions, dispensing cautions, and patient information warnings. The label also features the NDC code 24979-231-02 and a barcode.*

FDA Label Image

Image Description (Usl 10 1000)

Potassium Chloride Extended-Release Tablets USP 750 mg (10 mEq) film-coated tablets package label by Upsher-Smith Laboratories, LLC. The label states 1,000 tablets with prescription-only status and includes storage instructions, dosage details, and patient information warnings.*

FDA Label Image

Image Description (Potassium 03)

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.*

FDA Label Image

Image Description (Usl 20 100)

Potassium Chloride Extended-Release Tablets, USP 20 mEq (1,500 mg), film-coated, 100 count bottle label from Upsher-Smith Laboratories, LLC. The label includes cautionary storage instructions, dosage directions, and a barcode with NDC 24979-232-01. It advises not to accept if the seal is broken or missing and to store at controlled room temperature.*

* 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.