Potassium Chloride Tablet, Extended Release
Product Images NDC 72865-196

3 FDA label images from Xlcare Pharmaceuticals, Inc. · 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 72865-196). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xlcare Pharmaceuticals, 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

10 Meq K- 500s Count (10 Meq K 500s)

10 Meq K- 500s Count (10 Meq K 500s)
Label for Potassium Chloride Extended-Release Tablets, USP, 750 mg (10 mEq K) oral tablets by XLCare Pharmaceuticals, Inc. The package contains 500 tablets. The label includes storage instructions to keep the product at 20° to 25°C, warning to protect from light and moisture, and notes dispensing in a tight, light-resistant container. It is marked Rx only and displays a barcode with lot and expiration date fields.*
FDA Label Image

15 Meq K- 500s Count (15 Meq K 500s)

15 Meq K- 500s Count (15 Meq K 500s)
Potassium Chloride Extended-Release Tablets USP, 1125 mg (15 mEq), by XLCare Pharmaceuticals Inc. The label shows a bottle containing 500 tablets with Rx-only status. Key storage instructions and manufacturer information for Ascent Pharmaceuticals are included on the label, along with regulatory and dosage notes.*
FDA Label Image

20 Meq K- 500s Count (20 Meq K 500s)

20 Meq K- 500s Count (20 Meq K 500s)
Potassium Chloride Extended-Release Tablets USP 1500 mg (20 mEq K) oral tablets in a 500 count package by XLCare Pharmaceuticals Inc. The label includes storage, dosage, and manufacturing information along with a barcode and lot/expiration date fields.*

* 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.