Ilumya Injection, Solution
Product Images NDC 47335-177

4 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ilumya (NDC 47335-177). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Image-1 (Ilumya1)

Image-1 (Ilumya1)
An instructional diagram of the ILUMYA 100 mg/mL prefilled syringe for subcutaneous injection. The image labels key syringe parts including the needle cover, needle guard, syringe body, dose window, finger grip, and blue plunger. A caution advises not to pull off the needle cover until ready to inject.*
FDA Label Image

Image-2 (Ilumya2)

Image-2 (Ilumya2)
An instructional illustration showing a hand administering a subcutaneous injection with a syringe, indicated by an arrow pointing into the skin. No product-specific text or labels are visible in the image.*
FDA Label Image

Image-3 (Ilumya3)

Image-3 (Ilumya3)
An instructional illustration showing a hand holding a prefilled syringe for injection. An arrow indicates pulling the plunger back to draw fluid or prepare the syringe for subcutaneous injection, related to the administration of ILUMYA (tildrakizumab-asmn) injection solution.*
FDA Label Image

Image-4 (Ilumya4)

Image-4 (Ilumya4)
ILUMYA 100 mg/mL (tildrakizumab-asmn) injection label for subcutaneous use. The label indicates a single-dose prefilled syringe with sterile solution containing no preservative. The packaging advises dispensing the enclosed Medication Guide and discarding any unused portion. It includes a syringe illustration and states contents as one 1-mL single-dose prefilled syringe with prescribing information and medication guide. Labeler is Sun Pharmaceutical Industries, Inc.*

* 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.