Potassium Chloride Tablet, Extended Release
Product Images NDC 60687-756

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 60687-756). 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.

Product Images & Figures Index

FDA Label Image

20 Meq Potassium Chloride Er Tablet Blister (20 Meq Potassium Chloride Er Tablet Blister)

20 Meq Potassium Chloride Er Tablet Blister (20 Meq Potassium Chloride Er Tablet Blister)
Potassium Chloride 20 mEq extended-release oral tablets in a blister pack. Each individual tablet is labeled with the proprietary name, strength, dosage form, and includes a barcode, lot number, and expiration date area. The labeler is American Health Packaging.*
FDA Label Image

20 Meq Potassium Chloride Er Tablets Carton (20 Meq Potassium Chloride Er Tablets Carton)

20 Meq Potassium Chloride Er Tablets Carton (20 Meq Potassium Chloride Er Tablets Carton)
Label for Potassium Chloride Extended-Release Tablets, USP, 20 mEq strength, oral dosage form. The label states 80 tablets per package and the product is prescription only. It includes the NDC number 60687-756-09, distributor American Health Packaging in Columbus, Ohio, and storage instructions along with safety warnings.*
FDA Label Image

Ahp75609

Ahp75609
Potassium Chloride 20 meq extended release oral tablet, white and oblong with scored line on one side and embossed imprint 'Andrx 720' on the other side. No packaging or labeling visible beyond the tablet itself.*

* 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.