Qalsody Injection
Product Images NDC 64406-109

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Qalsody (NDC 64406-109). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Biogen 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.

FDA Label Image

Figure 1 (Qal00 0004 01)

Chemical structure diagram of the active ingredient tofersen. The schematic shows the molecular composition including various nucleotide components and the structural backbone details.*

FDA Label Image

Figure 2 (Qal00 0004 02)

A line graph comparing the LS Geometric Mean Ratio to Baseline of a measure labeled PK in two groups over 28 study weeks. One group, labeled as placebo (N=36), is represented by a blue dashed line with round markers, while the other group, labeled QALSODY 100 mg (N=72), is shown with a solid red line with square markers. Data points include error bars indicating variability at each study week.*

FDA Label Image

Principal Display Panel (Carton Label)

QALSODY (tofersen) Injection 100 mg/15 mL (6.7 mg/mL) sterile solution for intrathecal injection only. The packaging indicates a single-dose vial with usage instructions and storage information. It is labeled Rx only and manufactured by Biogen Inc. in Cambridge, MA. The label includes dosage details, ingredients, and a barcode.*

FDA Label Image

Principal Display Panel (Vial Label)

Label for QALSODY (tofersen) Injection, 100 mg/15 mL (6.7 mg/mL) sterile solution for intrathecal injection only. The label indicates it is a single-dose vial, to be stored refrigerated between 2°C to 8°C (36°F to 46°F), and includes handling instructions. Manufactured for Biogen MA Inc., Cambridge, MA.*

* 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.