Ferric Citrate Tablet, Film Coated
Product Images NDC 0378-2895

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 Ferric Citrate (NDC 0378-2895). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals 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.

FDA Label Image

Chemical Formula (Image 01)

Chemical Formula (Image 01)
Chemical structure of ferric citrate showing ferric (Fe3+) ion complexed with citrate ions, along with hydrated water molecules (y H2O) and specified ranges for x and y values indicating variable hydration and stoichiometry.*
FDA Label Image

Figure 1: Serum Phosphorus Control Over 52 Weeks (Image 02)

Figure 1: Serum Phosphorus Control Over 52 Weeks (Image 02)
A line graph comparing mean serum phosphorus levels (mg/dL) over a 52-week active-controlled study period between Ferric Citrate and an active control. The x-axis shows time points from Baseline through Week 52, and the y-axis represents mean serum phosphorus with error bars at each time point for both groups, demonstrating trends over time.*
FDA Label Image

210 mg Bottle Label (Image 03)

210 mg Bottle Label (Image 03)
Ferric Citrate 210 mg film-coated tablets packaging label by Mylan Pharmaceuticals Inc. The label displays the NDC 0378-2895-20 and indicates 200 tablets per container. It includes storage instructions, a warning about accidental overdose, and advises seeing the package insert for dosage information. The label also notes the product is made in France and contains FD&C Yellow No. 6.*

* 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.