Naloxone Hydrochloride Injection
Product Images NDC 42023-224

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 42023-224). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Par Health 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

Structural Formula (Naloxone Hydrochloride Injection Usp 1)

Chemical structure of Naloxone Hydrochloride showing the molecular rings and key functional groups including hydroxyls and a chlorine atom associated with the hydrochloride salt.*

FDA Label Image

Prior To Assembly Image (Naloxone Hydrochloride Injection Usp 2)

Illustration showing components of a syringe used for Naloxone Hydrochloride injection, including labeled parts: Tip Cap, Glass Barrel, Plunger Stopper, and Plunger Rod.*

FDA Label Image

Pre-filled Syringe Image (Naloxone Hydrochloride Injection Usp 3)

An instructional diagram showing a syringe with labeled parts: Tip Cap, Glass Barrel, Plunger Stopper, and Plunger Rod. The plunger rod is pulled back, indicated by a left-pointing arrow. This schematic details the syringe components typically used for Naloxone Hydrochloride injection.*

FDA Label Image

Unit Carton (Naloxone Hydrochloride Injection Usp 4)

Packaging label for Naloxone Hydrochloride Injection, USP, 2 mg per 2 mL (1 mg/mL) solution by Par Health USA, LLC. The label includes dosage and usage details for intravenous, intramuscular, or subcutaneous administration as an opioid antagonist. It indicates the product is preservative-free and the needle is not included. The label also contains storage instructions, inactive ingredients, and distributor information.*

* 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.