Auryxia Tablet, Film Coated
Product Images NDC 59922-631

3 FDA label images from Akebia Therapeutics, Inc. · 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 Auryxia (NDC 59922-631). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akebia Therapeutics, Inc., 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

Ferric Citrate Structure (Keryx Figure 1)

Ferric Citrate Structure (Keryx Figure 1)
Chemical structure of ferric citrate, the active ingredient in Auryxia tablets. The diagram shows the ferric ion (Fe+3) complexed with citrate ligands and associated water molecules, indicating variable stoichiometric coefficients x and y.*
FDA Label Image

Figure 1: Serum Phosphorus Control Over 52 Weeks (Keryx Figure 2)

Figure 1: Serum Phosphorus Control Over 52 Weeks (Keryx Figure 2)
A line graph showing mean serum phosphorus levels (mg/dL) over a 52-week period comparing Active Control and Ferric Citrate groups. Mean serum phosphorus decreases from baseline to week 12, then remains relatively stable through week 52 for both groups, with overlapping confidence intervals at each time point.*
FDA Label Image

Bottle Label (Keryx Figure 3)

Bottle Label (Keryx Figure 3)
Auryxia (ferric citrate) 210 mg film-coated tablets label showing 200 tablets per package. The label includes storage instructions, overdose warning, and manufacturer information for Akebia Therapeutics, Inc. It also contains NDC 59922-631-01 and advises checking package insert for dosage details.*

* 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.