Potassium Chloride Tablet
Product Images NDC 43547-550

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 43547-550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solco Healthcare 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

Container Label 750 mg (Image 01)

Container Label 750 mg (Image 01)
Label for Potassium Chloride Extended-Release Tablets, USP 750 mg oral tablets. The package contains 100 tablets and is labeled by Solco Healthcare LLC. The label includes dosage information, storage instructions, and manufacturer details from Zhejiang Huahai Pharmaceutical Co., Ltd. The product is marked for prescription use only with NDC 43547-549-10.*
FDA Label Image

Container Label 1125 mg (Image 02)

Container Label 1125 mg (Image 02)
Label for Potassium Chloride Extended-Release Tablets, USP, 1125 mg (15 mEq potassium), oral tablets. The label shows 100 tablets per container, distributed by Solco Healthcare LLC. Storage instructions and manufacturer information for Zhejiang Huahai Pharmaceutical Co., Ltd. are included. The label includes a barcode and a note indicating prescription use only.*
FDA Label Image

Container Label 1500 mg (Image 03)

Container Label 1500 mg (Image 03)
Potassium Chloride Extended-Release Tablets USP 1500 mg oral tablets in a blue and white rectangular label. The label indicates 20 mEq potassium content, the NDC number 43547-550-10, and packaging of 100 tablets. Manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd and distributed by Solco Healthcare LLC in Somerset, NJ.*

* 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.