Potassium Chloride Tablet, Extended Release
Product Images NDC 72603-337

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 72603-337). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

750 mg (Figure A)

750 mg (Figure A)
This text consists of information about a potassium chloride extended-release tablet, containing 750 mg of potassium. It mentions the usual dosage and instructions for administration, including keeping the tablets in a tight container and out of the reach of children. The tablets are manufactured by Ascent Pharmaceuticals under the NORTHSTARS brand. The full prescribing information can be found in the package insert.*
FDA Label Image

1500 mg (Figure B)

1500 mg (Figure B)
This text provides information about extended-release potassium chloride tablets, each containing 1,500 mg of Potassium chloride, USP (equivalent to 20 mEq potassium). The usual dosage and details for prescribing can be found in the package insert. Dosage adjustment is necessary based on individual patient needs. The tablets should be stored at room temperature (15-25°C or 66-77°F) in a tightly closed container and kept out of reach of children. The product is manufactured by Ascent Pharmaceuticals, Inc. for Northstar Rx LLC in Central Islip, NY.*

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