Ketamine Hydrochloride Injection, Solution
Product Images NDC 25021-682

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ketamine Hydrochloride (NDC 25021-682). 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

Figure (Ket0r 0000 01)

Chemical structure of Ketamine Hydrochloride showing a cyclohexanone ring linked to a chlorophenyl group and a methylamino substituent, along with the hydrochloride salt component.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Ket0r 0000 02)

Label for Ketamine Hydrochloride Injection, USP, 200 mg per 20 mL (10 mg per mL) solution. It is a 20 mL multi-dose vial for slow intravenous or intramuscular use. The label includes storage instructions, manufacturer details (Sagent Pharmaceuticals), lot and expiration fields, and barcodes.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Ket0r 0000 03)

Label for Ketamine Hydrochloride Injection, USP, 500 mg per 10 mL (50 mg/mL) solution for injection. The label indicates slow intravenous or intramuscular use in a 10 mL multi-dose vial, manufactured for Sagent Pharmaceuticals. It includes storage instructions, usage warnings, and a barcode.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Ket0r 0000 04)

Label for Ketamine Hydrochloride Injection, USP, 500 mg per 5 mL (100 mg per mL) solution. It states use for slow intravenous or intramuscular injection. The label shows it is a 5 mL multi-dose vial and includes storage instructions, manufacturer Sagent Pharmaceuticals, and NDC 25021-684-05.*

* 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.