Vyvgart Injection
Product Images NDC 73475-3041

3 FDA label images from Argenx Us · 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 Vyvgart (NDC 73475-3041). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Argenx Us, 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 1 (Vyvgart 01)

Figure 1 (Vyvgart 01)
A line graph comparing the mean change over weeks between VYVGART and placebo groups. The x-axis shows weeks from 0 to 10, and the y-axis shows mean change with standard error bars. VYVGART shows a larger decrease in mean change compared to placebo throughout the period.*
FDA Label Image

Figure 2 (Vyvgart 02)

Figure 2 (Vyvgart 02)
Two bar charts comparing the percentage of patients showing improvements in Total MG-ADL and Total QMG scores at Week 4. Each chart displays improvements across numeric categories and includes separate bars for VYVGART (black) and placebo (white). The charts also show percentages for 'No Change' and 'Worsening' outcomes for both groups.*
FDA Label Image

Principal Display Panel (20 mL Vial Carton)

Principal Display Panel (20 mL Vial Carton)
Packaging label for VYVGART (efgartigimod alfa-fcab) injection 400 mg/20 mL (20 mg/mL) by argenx US. The carton indicates it is for intravenous use only, requiring dilution before use in a 20 mL single-dose vial. Storage instructions specify refrigeration at 2°C to 8°C (36°F to 46°F), with warnings not to freeze or shake. The label includes the NDC 73475-3041-5 and barcodes, along with manufacturing and distribution details.*

* 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.