Sevelamer Carbonate Tablet, Film Coated
Product Images NDC 68094-034

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sevelamer Carbonate (NDC 68094-034). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Precision Dose, 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 Structure (Sevelamer 01)

Chemical structure diagram of Sevelamer Carbonate, showing the polymeric backbone with amine groups and bicarbonate ions, representing its active ingredient.*

FDA Label Image

Figure 3 (Sevelamer 02)

A cumulative distribution plot showing the percentage of patients with reductions in serum phosphorus levels (mg/dL) on the x-axis and the percentage of patients achieving at least those reductions on the y-axis. The graph compares Sevelamer Hydrochloride with an active control, illustrating patient response in terms of worsened increase versus improved reduction from baseline serum phosphorus.*

FDA Label Image

Figure 4 (Sevelamer 03)

A line graph showing phosphorus change from baseline over a 52-week study period. The graph compares two treatments: Sevelamer Hydrochloride and an Active-Control, with phosphorus change values plotted against study weeks.*

FDA Label Image

Principal Display Panel (800 mg Tablet Blister Pack Carton)

Label for Sevelamer Carbonate film-coated tablets, 800 mg strength, packaged by Precision Dose, Inc. The label indicates a unit dose package containing 90 tablets (9x10) with storage instructions and a barcode at the bottom. It specifies active ingredient strength and typical storage conditions.*

* 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.