Ketamine Hydrochloride Injection
Product Images NDC 65219-186

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ketamine Hydrochloride (NDC 65219-186). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, 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

Chemical Structure (Ket0t 0000 01)

Chemical Structure (Ket0t 0000 01)
Chemical structure of ketamine hydrochloride, showing its characteristic chlorophenyl group, cyclohexanone ring, and methylamino substituent along with the hydrochloride component.*
FDA Label Image

Logo (Ket0t 0000 02)

FDA Label Image

Logo (Ket0t 0000 03)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Ketamine HCl Injection, USP 5 mL Vial Label)

Package Label (PRINCIPAL DISPLAY – Ketamine HCl Injection, USP 5 mL Vial Label)
Label for Ketamine Hydrochloride Injection, USP Concentrate 100 mg/mL (500 mg/5 mL) by Fresenius Kabi USA, LLC. The label indicates it is a 5 mL multiple-dose vial for slow intravenous or intramuscular use, with a warning that it must be diluted prior to IV use. Includes dosage note and storage instructions.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Ketamine HCl Injection, USP 5 mL Tray Label)

Package Label (PRINCIPAL DISPLAY – Ketamine HCl Injection, USP 5 mL Tray Label)
Label for Ketamine HCl Injection USP Concentrate 500 mg/5 mL (100 mg/mL), intended for slow intravenous or intramuscular use. The product must be diluted prior to IV use and comes in 5 mL multiple-dose vials (10 per package). Manufactured by Fresenius Kabi USA, LLC under the PREMIER PRO Rx brand.*

* 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.