Tecelra Injection, Suspension
Product Images NDC 87262-160

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tecelra (NDC 87262-160). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Uswm Ct, 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

Principal Display Panel (Bag and Cassette Label)

Label for TECELRA (afamitresgene autoleucel) injection, suspension for intravenous use, by USWM CT, LLC. The label states it contains genetically modified cells (MAGE-A4 TCR positive T cells) in frozen suspension with 5% DMSO, and provides storage instructions at -130°C. It includes warnings about autologous use only, and not to use a leukodepleting filter or irradiate the product.*

FDA Label Image

Teclelra-bag Patient Info (Tecelra Bag)

Label for TECELRA (afamitresgene autoleucel) cellular therapy injection, suspension, intravenous. The label includes patient and product identifiers with barcodes, placeholders for patient first and last names, date of birth, and lot and expiration information. The labeler is USWM CT, LLC.*

FDA Label Image

Tecelra-cassette Patient Info (Tecelra Cass)

Label for TECELRA afamitresgene autoleucel injection, suspension for intravenous use by USWM CT, LLC. Prominently features a red stop sign with the warning to confirm patient identifiers prior to infusion. Includes placeholders for patient information such as MRN, COID, name, date of birth, and lot number, along with a barcode and expiration date December 31, 2024.*

* 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.