Melphalan Hydrochloride Kit
Product Images NDC 25021-258

View Photos of 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 Melphalan Hydrochloride (NDC 25021-258). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Structural Formula (Mel0c 0000 01)

Structural Formula (Mel0c 0000 01)
Chemical structure diagram of Melphalan Hydrochloride showing its molecular composition including the aromatic ring and functional groups typical of this compound.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Mel0c 0000 02)

Package Label – Principal Display Panel – Vial Label (Mel0c 0000 02)
Label for Melphalan Hydrochloride for Injection 50 mg per vial, an intravenous infusion single-use vial. The label indicates it is sterile, preservative-free, and cytotoxic. It is labeled for Sagent Pharmaceuticals, made in India, with storage instructions and a caution for cytotoxicity. The label includes a barcode and lot/expiration date fields.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Mel0c 0000 03)

Package Label – Principal Display Panel – Vial Label (Mel0c 0000 03)
Label for Melphalan Hydrochloride Diluent for Injection, 10 mL vial, by Sagent Pharmaceuticals. The label states the product is sterile, nonpyrogenic, and preservative-free, containing sodium citrate, propylene glycol, ethanol, and water. It is for drug diluent use only, with storage instructions and barcodes included. Manufactured in India for Sagent Pharmaceuticals, Schaumburg, IL.*

* 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.