Potassium Chloride Tablet, Extended Release
Product Images NDC 51655-706

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 51655-706). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 706 52 Master Bottle Label Approval Rev A 04 21)

Label (51655 706 52 Master Bottle Label Approval   Rev A 04 21)
This is a medication label for Potassium Chloride Extended-Release tablets, with 750 mg of the active ingredient per tablet. The medication is only available through prescription, and the dosage information can be found in the package insert. The label warns to keep out of reach of children, store at room temperature, protect from light and moisture, and notes that the expended matrix is not absorbed and may be excreted intact in stool. The medication contains FD&C Yellow No. 5 and is repackaged by Northwind Pharmaceuticals. The lot number is 0000000000, and the medication expires on 00/00/0000.*

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