Itvisma Injection, Suspension
Product Images NDC 71894-200

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Itvisma (NDC 71894-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novartis Innovative Technologies 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.

Product Images & Figures Index

FDA Label Image

Principal Display Panel Ndc 71894-200-02 Rx Only Onasemnogene Abeparvovec-brve Itvisma® Injection 1.2 × 1014 Vector Genomes/ 3 mL (4 X 1013 Vector Genomes (vg)/ml) Sterile Solution For Intrathecal Injection Only One Single-dose Vial Must Use Within 14 Days Of Receipt Do Not Shake | Do Not Refreeze Novartis (Itvisma 01)

Principal Display Panel							Ndc 71894-200-02							Rx Only							Onasemnogene							Abeparvovec-brve							Itvisma®							Injection							1.2 × 1014 Vector Genomes/ 3 mL							(4 X 1013 Vector Genomes (vg)/ml)							Sterile Solution For Intrathecal Injection Only							One Single-dose Vial							Must Use Within 14 Days Of Receipt							Do Not Shake | Do Not Refreeze							Novartis (Itvisma 01)
The packaging label for ITVISMA (onasemnogene abeparvovec-brve) injection, suspension displays the product name and active ingredient prominently. It indicates a strength of 1.2 x 10^14 vector genomes per 3 mL (4 x 10^13 vector genomes per mL). The label notes that this sterile suspension is for intrathecal injection only, provided as a single-dose vial, and must be used within 14 days of receipt. The manufacturer is Novartis Innovative Technologies Inc. The label also includes storage instructions to not shake or freeze and contains dosage and handling information.*

* 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.