Ketamine Hydrochloride
Product Images NDC 0409-0040

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 Ketamine Hydrochloride (NDC 0409-0040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Chemical Structure (Ketamine Hydrochloride 01)

Chemical Structure (Ketamine Hydrochloride 01)
Chemical structure diagram of Ketamine Hydrochloride showing its molecular framework with a cyclohexanone ring, chlorophenyl group, and methylamino substituent along with the hydrochloride (HCl) component.*
FDA Label Image

Logo (Ketamine Hydrochloride 02)

FDA Label Image

Principal Display Panel (5 mL Vial Label)

Principal Display Panel (5 mL Vial Label)
Label for Ketamine Hydrochloride Injection, USP 500 mg/5 mL (100 mg/mL) concentrate in a 5 mL multiple-dose vial by Hospira, Inc. The label indicates it is Rx only, for slow intravenous or intramuscular use, and must be diluted prior to intravenous use. It includes detailed concentration, usage instructions, storage conditions, and lot/expiration placeholders.*
FDA Label Image

Principal Display Panel (5 mL Vial Box)

Principal Display Panel (5 mL Vial Box)
Packaging label for Ketamine Hydrochloride Injection, USP by Hospira, Inc., featuring a 500 mg/5 mL (100 mg/mL) concentrate. The label indicates 5 mL x 10 multiple-dose vials per package, with instructions for slow intravenous or intramuscular use and a warning that the product must be diluted prior to intravenous use. The label also includes storage instructions, a barcode, and branding for Novaplus.*

* 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.