Deferoxamine Mesylate
Product Images NDC 52609-4504

3 FDA label images from Apopharma Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Deferoxamine Mesylate (NDC 52609-4504). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apopharma Usa, 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

Deferoxamine01 (Deferoxamine01)

Deferoxamine01 (Deferoxamine01)
Chemical structure of deferoxamine mesylate showing its molecular composition with multiple amide and hydroxyl functional groups.*
FDA Label Image

Deferoxamine500mg (Deferoxamine02)

Deferoxamine500mg (Deferoxamine02)
Deferoxamine mesylate for Injection, USP 500 mg per vial label from ApoPharma USA, Inc. The label indicates the drug is for subcutaneous, intramuscular, or intravenous administration with each vial containing 500 mg of lyophilized deferoxamine mesylate USP. The packaging contains 4 vials. Manufacturer and distributor details are included, along with storage instructions and a barcode.*
FDA Label Image

Deferoxamine2g (Deferoxamine03)

Deferoxamine2g (Deferoxamine03)
Drug label text panels for Deferoxamine Mesylate for Injection, USP. The label indicates a strength of 2 g per vial in lyophilized form for subcutaneous, intramuscular, or intravenous administration. The panels include dosage instructions, storage conditions, manufacturer and distributor information, and product warnings. The labeler is ApoPharma USA, Inc., with four vials per package.*

* 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.