Potassium Citrate Tablet, Extended Release
Product Images NDC 72162-2122

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 Citrate (NDC 72162-2122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Structure (Structure)

Structure (Structure)
Chemical structure of potassium citrate monohydrate showing the arrangement of carbon, hydrogen, oxygen, and potassium atoms, with the molecular formula including water of hydration (H2O).*
FDA Label Image

Table 1. (Table 1.)

Table 1. (Table 1.)
A data table titled "Effect of Potassium Citrate In Patients With Calcium Oxalate Nephrolithiasis" showing the number of stones formed per year across different patient groups. Columns include Baseline, On Treatment, Remission percentage, and Any Decrease percentage for four groups (I-IV) and total patients (n=89). A footnote defines remission as the percentage of patients free of newly formed stones during treatment.*
FDA Label Image

Label (Lbl721622122)

Label (Lbl721622122)
Label for Potassium Citrate Extended-Release Tablets USP, 5 mEq (540 mg) per tablet, in a bottle of 100 tablets. The label includes the NDC 72162-2122-1 and states the tablets are uncoated, round, off white to tan yellowish, and debossed with 'T' and '399'. The labeler is Bryant Ranch Prepack, with manufacturing by Ascent Pharmaceuticals.*

* 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.