Ilumya Injection, Solution
Product Images NDC 47335-177

View Photos of 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.

FDA Label Image

Ilumya 1

Ilumya 1
An instructional diagram of the ILUMYA prefilled syringe for subcutaneous injection, illustrating labeled parts including the needle cover, needle guard, syringe body, dose window, finger grip, and blue plunger. The image includes a caution not to pull off the needle cover until ready to inject.*
FDA Label Image

Ilumya 2

Ilumya 2
An illustration showing a hand holding a syringe at an angle, preparing for a subcutaneous injection, consistent with the administration method of ILUMYA (tildrakizumab-asmn) injection solution, 100 mg/mL.*
FDA Label Image

Ilumya 3

Ilumya 3
An instructional illustration depicting a hand holding a syringe with an arrow indicating the removal of a cap from the syringe needle. This suggests preparation for a subcutaneous injection.*
FDA Label Image

Ilumya 4

Ilumya 4
ILUMYA 100 mg/mL (tildrakizumab-asmn) injection label for a subcutaneous solution. The label includes instructions for subcutaneous use, dispensing a medication guide, and discarding unused portions. It depicts a syringe illustration and notes the contents include a 1 mL single-dose prefilled syringe, prescribing information, and a medication guide. The 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.