Ferabright Injection
Product Images NDC 24338-510

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ferabright (NDC 24338-510). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Azurity Pharmaceuticals, 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

Spl-10ml-carton (Spl 10ml Carton)

Packaging label for FeraBright (ferumoxytol injection) 30 mg/mL, a human prescription drug for intravenous injection. The label highlights 300 mg elemental iron per 10 mL and indicates it is for intravenous use after dilution only. Manufactured by Azurity Pharmaceuticals, Inc., the package contains one single-dose vial with instructions to discard any unused portion.*

FDA Label Image

Spl-10ml-label (Spl 10ml Label)

Label for FeraBright (ferumoxytol injection) 30 mg/mL, a single-dose vial for intravenous use after dilution. The label states 300 mg elemental iron per 10 mL. Manufactured for Azurity Pharmaceuticals, the label includes storage instructions and notes the product is Rx only.*

FDA Label Image

Spl-17ml-carton (Spl 17ml Carton)

Packaging label for FeraBright (ferumoxytol injection) 30 mg/mL, an intravenous injection. The label states 510 mg elemental iron per 17 mL and indicates the product is for intravenous use after dilution only. The labeler is Azurity Pharmaceuticals, Inc. It also includes storage instructions, a barcode, and the NDC 24338-510-17 for a single-dose vial.*

FDA Label Image

Spl-17ml-label (Spl 17ml Label)

Label for FeraBright (ferumoxytol injection) 30 mg/mL single-dose vial by Azurity Pharmaceuticals. The label states 510 mg elemental iron per 17 mL for intravenous use after dilution only. It includes storage instructions and mentions that the vial is single-dose with unused portion discarded. The label features the Azurity Pharmaceuticals logo and regulatory details including lot and expiration placeholders.*

* 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.