Dexrazoxane Injection, Powder, Lyophilized, For Solution
Product Images NDC 68083-195

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 Dexrazoxane (NDC 68083-195). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Dexrazoxane-image1 (Dexrazoxane Image1)

Dexrazoxane-image1 (Dexrazoxane Image1)
Chemical structure diagram of Dexrazoxane, the active ingredient in Dexrazoxane for Injection.*
FDA Label Image

Dexrazoxane-image2 (Dexrazoxane Image2)

Dexrazoxane-image2 (Dexrazoxane Image2)
Bar graph comparing the number of patients in treatment groups receiving FAC/Dexrazoxane and FAC alone by cumulative dose of Doxorubicin in mg/m². The x-axis shows increasing dose ranges from 350 up to 1000+ mg/m², while the y-axis represents the number of patients from 0 to 120. White bars indicate FAC/Dexrazoxane, black bars indicate FAC.*
FDA Label Image

Image3 (Dexrazoxane Image3)

Image3 (Dexrazoxane Image3)
Label for Dexrazoxane for Injection 500 mg per vial, sterile, pyrogen-free, lyophilized powder for intravenous use only. The single dose vial label includes dosing preparation instructions, storage conditions (2 to 25 degrees Celsius), and manufacturer information from Gland Pharma Limited. The label also features a barcode and regulatory statements including Rx Only and lot/expiration fields.*
FDA Label Image

Image4 (Dexrazoxane Image4)

Image4 (Dexrazoxane Image4)
Packaging label for Dexrazoxane for Injection 500 mg per vial, sterile, pyrogen-free, lyophilized powder for solution. The label states it is a single-dose vial for intravenous use only. It is manufactured by Gland Pharma Limited, Hyderabad, India. The label includes lot and expiration fields, dosage reconstitution instructions, and a barcode.*

* 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.