Nephroscan Injection, Powder, Lyophilized, For Solution
Product Images NDC 71083-0020

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nephroscan (NDC 71083-0020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Theragnostics 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

Image (Nephroscan 01)

An illustration showing migration distances on a thin-layer chromatography strip for Technetium Tc 99m compounds. It labels the solvent front, origin, and Rf values for unbound free Tc 99m, Technetium Tc 99m succimer, and hydrolyzed Tc 99m, with an explanation of the Rf calculation based on solvent and solute travel distances.*

FDA Label Image

Image (Nephroscan 02)

The image displays a formula defining Percent (%) Raciochemical Purity as a ratio involving Technetium Tc 99m succimer activity over total activity, which includes Tc 99m succimer, HR Tc 99m, and Unbound Tc 99m, multiplied by 100. This text panel relates to radiochemical purity measurements for a technetium-labeled succimer compound.*

FDA Label Image

Chemical Structure (Nephroscan 03)

Chemical structure of succimer shown as a molecular diagram, depicting its functional groups including thiol (SH) and carboxyl (COOH) groups.*

FDA Label Image

Principal Display Panel (1 mg Vial Carton)

NephroScan 1 mg per vial Succimer injection, powder, lyophilized for intravenous use. The packaging is a kit for preparation of Technetium Tc 99m Succimer Injection, labeled for 5 single-dose vials. Manufactured by Theragnostics Inc and ROTOP Pharmaka GmbH, the label includes storage instructions, vial contents, and a warning for qualified healthcare professional use only.*

* 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.