Tecelra Injection, Suspension
Product Images NDC 83205-0001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tecelra (NDC 83205-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Uswm, 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

Teclelra-bag (Tecelra Bag Princ)

Teclelra-bag (Tecelra Bag Princ)
This is a description of "afamitresgene autoleucel," a medication designed for autologous and intravenous use. It contains a specific dosage of MAGE-A4 TCR positive T cells in a frozen suspension with 5% DMSO. The product should be gently mixed post-thaw before intravenous infusion. It is important to follow the full prescribing information for administration. The medication must be stored and transported at or below -130°C. The product is genetically modified, and it is advised not to use a leukodepleting filter or irradiate it. It has not been evaluated for infectious substances. The manufacturer is Adsptmmune LLC based in Pennsylvania, USA. For more information or assistance, contact them at the provided phone number.*
FDA Label Image

Teclelra-bag Patient Info (Tecelra Bag)

Teclelra-bag Patient Info (Tecelra Bag)
The text provides information about a medical product called afamitresgene autoleucel with identifiers such as Patient MRN, COID, First Name, Last Name, OB, BIN, Exp, and Lot. The expiry date for this product is December 31, 2024. Additional details include alphanumeric codes such as VERFYPATENT.*
FDA Label Image

Tecelra-cassette Patient Info (Tecelra Cass)

Tecelra-cassette Patient Info (Tecelra Cass)
The text provides information about a medication called afamitresgene autoleucel, branded as Tecelra®. It includes a patient's unique identifiers such as MAN, COID, First Name, Last Name, DOB, and DIN for tracking and administration purposes. Additionally, there is a reference number (L8L00036Rev00) with an expiration date (31.Dec-2024) and lot number. The text emphasizes on confirming patient identifiers before administering the medication.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.