Ketamine Hydrochloride Injection
Product Images NDC 0404-9759

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 Ketamine Hydrochloride (NDC 0404-9759). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

Formula1.jpg (Formula1)

Formula1.jpg (Formula1)
Chemical structure of ketamine hydrochloride showing a cyclohexanone ring, chlorophenyl group, and methylamino substituent with the HCl component indicated separately.*
FDA Label Image

Image1.jpg (Image1)

Image1.jpg (Image1)
A data table listing product codes, units of sale, strengths (concentration), and units of use for ketamine hydrochloride injection. The table details three product codes with their respective NDC numbers, vial sizes, concentrations, and equivalents of ketamine base and ketamine hydrochloride in multiple-dose vials ranging from 5 mL to 20 mL.*
FDA Label Image

Label1.jpg (Label1)

Label1.jpg (Label1)
KETAMINE HCL 500 mg/5 mL injection vial label. This concentrate contains 100 mg/mL ketamine hydrochloride for slow intravenous or intramuscular use. The 6 mL vial is manufactured by Henry Schein, Inc. Directions indicate the solution must be diluted before IV use. Storage instructions include 20 to 25°C with protection from light and freezing. The label also displays NDC 0404-9759-05, lot number, expiration date, and manufacturer address.*

* 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.