Cisplatin Injection, Solution
Product Images NDC 0703-5747

3 FDA label images from Teva Parenteral Medicines, 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 Cisplatin (NDC 0703-5747). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Parenteral Medicines, 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

Cisplatin Injection Solution A074656 1

Cisplatin Injection Solution A074656 1
Chemical structure of the active ingredient cisplatin, showing a platinum (Pt) atom coordinated with two chlorine (Cl) atoms and two ammonia (NH3) groups in a square planar arrangement.*
FDA Label Image

Cisplatin Injection Solution A074656 2

Cisplatin Injection Solution A074656 2
Packaging label for Cisplatin Injection, 50 mg/50 mL (1 mg/mL) sterile solution for intravenous use. The label includes dosage warnings, storage instructions, and manufacturer information indicating Teva Parenteral Medicines, Inc. It also highlights the requirement to protect the container from light and not refrigerate, and includes barcodes on the packaging.*
FDA Label Image

Cisplatin Injection Solution A074656 3

Cisplatin Injection Solution A074656 3
Label for Cisplatin Injection 100 mg/100 mL (1 mg/mL) sterile solution for intravenous use. The label includes dosage caution, storage instructions at 20° to 25°C, and warnings to keep out of reach of children. It is labeled Rx only and manufactured by Teva Parenteral Medicines, Inc. with manufacturing in the Netherlands. The label features the Teva logo 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.