Potassium Chloride Capsule, Extended Release
Product Images NDC 68001-396

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 68001-396). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Potassiun Chloride Er Capsules Usp 10meq 100's.jpg (Label)

The text describes a medication with National Drug Code 68001-396-00 that is only available with a prescription. The medication is Potassium Chloride, which is microencapsulated in Extended-Release Capsules, USP. The capsules contain 750 mg of potassium chloride and 10 mEq K. They are designed to release the active ingredient over an 8- to 10-hour period. The dosage information is provided in the accompanying package insert, and the medication should be dispensed in a tight container as defined by USP standards. The medication is manufactured by Glenmark Pharmaceuticals in India. It should be stored at 20° to 25°C with excursions permitted to 15° to 30°C. Contact information for questions is also provided.*

* 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.