Elzonris Injection, Solution
Product Images NDC 72187-0401

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Elzonris (NDC 72187-0401). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stemline Therapeutics, 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

1000 Mcgg/ml Vial Label (Elzonris 01)

1000 Mcgg/ml Vial Label (Elzonris 01)
N7/ ELZONRIS (tagraxofusp-erzs) injection is a medication that is diluted and administered intravenously, with a concentration of 1,000 mcg/mL. It is important to discard any unused portion of the single dose vial. This medication is produced by Stemline Therapeutics, Inc. and the product code is 72187-0401-1.*
FDA Label Image

1000 Mcgg/ml Carton Label (Elzonris 02)

1000 Mcgg/ml Carton Label (Elzonris 02)
ELZONRIS (tagraxofusp-erzs) injection is a medication that comes in a single-dose vial of 1,000 mcg/mL for intravenous infusion after dilution. It contains tagraxofusp-erzs, sodium chloride, sorbitol, tromethamine, and water for injection. ELZONRIS is used for treatment as prescribed by a doctor. The medication should be stored in a freezer between -25°C and -15°C and thawed between 15°C and 25°C for 15 to 30 minutes in the original carton. Thawed vials may be held at room temperature for approximately 1 hour prior to dosage preparation. The medication is manufactured and distributed by Stemline Therapeutics, Inc. For questions, call 8773327961.*

* 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.