Potassium Chloride Capsule, Extended Release
Product Images NDC 63304-090

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 63304-090). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Pdp-600mg-100 (Potassium 01)

Potassium Chloride Extended-Release Capsules, USP 600 mg, 100 count. The label states the capsules contain 8 mEq potassium and are designed for extended release over 8 to 10 hours. It is labeled for oral use, Rx only, and distributed by Sun Pharmaceutical Industries, Inc. The label includes storage instructions and manufacturer details for Adare Pharmaceuticals, Inc.*

FDA Label Image

Pdp-750mg-100 (Potassium 02)

Label for Potassium Chloride Extended-Release Capsules USP, 750 mg strength, providing 10 mEq potassium. The label includes dosage form as extended-release capsules and indicates the product is prescription-only with 100 capsules per container. Manufactured by Adare Pharmaceuticals and distributed by Sun Pharmaceutical Industries, Inc. The label features the Sun Pharma logo and a barcode.*

FDA Label Image

Pdp-750mg-500 (Potassium 03)

Label for Potassium Chloride Extended-Release Capsules, USP 750 mg with 10 mEq potassium, manufactured by Aardv Pharmaceuticals and distributed by Sun Pharmaceutical Industries, Inc. The label states it contains 500 capsules and includes storage instructions for 20° to 25°C. It features the Sun Pharma logo and the NDC number 63304-090-05.*

* 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.