Deferoxamine Mesylate Injection, Powder, Lyophilized, For Solution
Product Images NDC 60505-6237

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Deferoxamine Mesylate (NDC 60505-6237). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp., 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

2gm-vial (2gm Vial)

This is a pharmaceutical product used for SC, IM, or IV injection. It is a single-dose product and the package contains directions on how to reconstitute it. It should be stored at a controlled room temperature of 20° to 25°C. The product contains Deferoxamine Mesylate and has a net weight of 2 g per vial. It is manufactured by Gland Pharma Limited in Hyderabad, India, for Apotex Corp in Weston, FL, USA. The lot number is 10¥AP/RR/S7/E/R and the NDC is 60505-6237-0. The GTN number is 1030505623706. The product warns against using turbid solutions and also advises discarding unused portions.*

FDA Label Image

500mg-vial (500mg Vial)

Deferoxamine Mesylate for Injection, USP is a medication that can be used for subcutaneous, intramuscular, or intravenous administration. The NDC number for this medication is 60505-6236-0 and it is manufactured by a company called Gland Pharma Limited in Hyderabad, India. The medication is intended to be reconstituted prior to use and should be stored at a controlled room temperature. Specific cautionary instructions are provided on the packaging. The medication is distributed in a package that includes a 2D barcode which can be used for online tracking.*

FDA Label Image

Deferoxamine01 (Deferoxamine01)

* 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.