Naloxone Hydrochloride Injection, Solution
Product Images NDC 36000-308

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 36000-308). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Image 01

Label for Naloxone Hydrochloride Injection, USP 0.4 mg/mL in a 1 mL single-dose vial. Suitable for intravenous, intramuscular, or subcutaneous use. Manufactured for Baxter Healthcare Corporation, Deerfield, IL. The label includes storage instructions to protect from light and discard unused portion, with manufacturing origin listed as Taiwan.*

FDA Label Image

Image 02

Label for Naloxone Hydrochloride Injection, USP 0.4 mg/mL by Baxter Healthcare Corporation. The injection solution is indicated for intravenous, intramuscular, or subcutaneous use. The package contains 10 single-dose vials of 1 mL each. The label advises aseptic technique, storage conditions, and protection from light.*

FDA Label Image

Image 03

Naloxone Hydrochloride Injection, USP 0.4 mg/mL label for single-dose vials. The label states the product is for intravenous, intramuscular, or subcutaneous use and is sterile and nonpyrogenic. It includes a package size of 10 single-dose 1 mL vials and is labeled by Baxter Healthcare Corporation. The label also instructs to protect from light by retaining in the carton until ready for use and to discard unused portions.*

FDA Label Image

Image 04

Chemical structure of naloxone hydrochloride dihydrate showing the detailed molecular arrangement including aromatic rings, hydroxyl groups, and hydrochloride with two water molecules.*

* 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.