Elitek Kit
Product Images NDC 0024-5150

4 FDA label images from Sanofi-aventis U.s. Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Elitek (NDC 0024-5150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanofi-aventis U.s. Llc, 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

Figure (Elitek 01)

Figure (Elitek 01)
A box plot chart depicting plasma uric acid levels (mg/dL) over time in hours from the first dose of Elitek (rasburicase). Time points range from baseline to 96 hours, with sample sizes indicated below each time. The chart shows plasma uric acid concentration changes post-treatment over the specified time intervals.*
FDA Label Image

Figure (Elitek 02)

Figure (Elitek 02)
A box-and-whisker plot showing plasma uric acid levels (mg/dL) over time from the first dose (hours) for three treatment arms: Elitek, Elitek/Allopurinol, and Allopurinol. Time points include baseline through 144 hours, with data points marked for each treatment arm across these intervals.*
FDA Label Image

Principal Display Panel (1.5 mg Kit Carton)

Principal Display Panel (1.5 mg Kit Carton)
Elitek 1.5 mg kit containing rasburicase for intravenous infusion. The label indicates the product is sterile, contains no preservatives, and must be reconstituted and diluted before use with the accompanying diluent. The package includes three single-dose vials and three diluent ampules. Manufactured by Sanofi-Aventis U.S. LLC.*
FDA Label Image

Principal Display Panel (7.5 mg Kit Carton)

Principal Display Panel (7.5 mg Kit Carton)
Packaging label for Elitek rasburicase 7.5 mg kit for intravenous infusion. The label includes instructions to reconstitute with accompanying diluent before use and indicates the kit contains one single-dose vial and one diluent ampule. The product is labeled as Rx only and is manufactured by Sanofi-Aventis U.S. LLC.*

* 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.