Waskyra Injection
Product Images NDC 87233-0100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Waskyra (NDC 87233-0100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fondazione Telethon Ets, 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

Metalcassette (Image002)

Label for WASKYRA (etuvetidigene autotemcel) injection 1000000 U/mL by Fondazione Telethon ETS. The label includes detailed usage instructions for an autologous CD34+ cell population infusion, handling storage requirements, manufacturer AGC Biologics S.p.A. in Italy, and regulatory identifiers including NDC 87233-0100-1 and a barcode. The label features a Fondazione Telethon logo and contact address in Rome, Italy.*

FDA Label Image

Infusionbag (Image01)

WASKYRA (etuvetidigene autotemcel) injection label showing 1.9 - 11.4 x 10^6 CD34+ cells/mL dispersion for infusion. It is for intravenous use and autologous use only, packaged as a cryopreservative solution containing 5% DMSO. The label includes storage instructions below -130°C, bar code, lot, DIN, expiration fields, and manufacturer information for Fondazione Telethon ETS and AGC Biologics S.p.A. in Italy.*

FDA Label Image

Overwrapbag (Image03)

WASKYRA 1000000 U/mL injection label for intravenous use containing etuvetidigene autotemcel. The label includes dosing instructions, storage information to keep frozen below -130°C, and manufacturing details by Fondazione Telethon ETS and AGC Biologics S.p.A. It specifies autologous use only and contains a barcode with NDC 87233-0100-1.*

* 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.