Potassium Chloride Capsule, Extended Release
Product Images NDC 60687-653

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 60687-653). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp65301

FDA Label Image

(750 mg) 10 Meq K Potassium Chloride Extended-release Capsule Blister (Blister)

Potassium chloride extended-release capsules, USP, contain 750mg and deliver 10mEq K. The lot number and expiry date are printed on the capsule. The drug is intended for therapeutic use.*

FDA Label Image

(750 mg) 10 Meq K Potassium Chloride Extended-release Capsules Carton (Carton)

The text describes a drug named Potassium Chloride Extended-Release Capsules, USP that is sold in a bottle containing 100 capsules. Each capsule contains 750 mg of the active ingredient and is designed to release 10 mEq of KCl over 8-16 hours. The drug is only available via prescription and should be stored at temperatures between 20° and 25°C, with permissible excursions between 16° to 30°C. The drug is distributed by American Health Packaging and cannot be used if the blister or packaging is broken. The information identifies the manufacturer as Sun Pharmaceutical Industries, Inc. The NDC number specified is 60687-653-01.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.