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

3 FDA label images from American Health Packaging · 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 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

Ahp65301
POTASSIUM CHLORIDE 750 mg extended-release oral capsule in light blue color. One side of the capsule is marked with the imprint "103" while the other side is blank. The capsule is manufactured by American Health Packaging.*
FDA Label Image

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

(750 mg) 10 Meq K Potassium Chloride Extended-release Capsule Blister (Blister)
Multiple identical labels for Potassium Chloride Extended-Release Capsules, USP 750 mg, 10 mEq potassium, manufactured by American Health Packaging. Each label displays the drug name, strength, dosage form, National Drug Code (NDC) 60687-653-11, barcode, and placeholders for lot number and expiry date.*
FDA Label Image

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

(750 mg) 10 Meq K Potassium Chloride Extended-release Capsules Carton (Carton)
Potassium Chloride Extended-Release Capsules, USP 750 mg with 10 mEq potassium, supplied as 100 capsules (10 x 10) in a single package. The label includes usage and storage information, and lists American Health Packaging as the distributor in Columbus, Ohio.*

* 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.