Naloxone Hydrochloride Injection
Product Images NDC 76329-3369

4 FDA label images from International Medication Systems, Limited · 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 Naloxone Hydrochloride (NDC 76329-3369). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by International Medication Systems, Limited, 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

Instructions (Instructions)

Instructions (Instructions)
An instructional illustration showing three steps for using an injection device with a vial. The steps include removing protective caps and aligning the vial with the injector needle, threading the vial into the injector with 3 half turns until the needle penetrates the stopper (with a warning not to push the vial into the injector), and removing the needle cap and expelling air before injection.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Naloxone Hydrochloride, showing the molecular arrangement including aromatic rings, hydroxyl groups, and a hydrochloride component.*
FDA Label Image

Carton 1469

Carton 1469
Naloxone Hydrochloride injection, USP 1 mg/mL (2 mg/2 mL) prefilled syringe by International Medication Systems, Limited. The label indicates the product is for intravenous, intramuscular, or subcutaneous use as an opioid antagonist. It includes usage instructions, warnings against syringe reuse, and packaging details such as NDC 76329-1469-1 and stock number 1469.*
FDA Label Image

Carton 3369

Carton 3369
Naloxone Hydrochloride Injection, USP 1 mg/mL in a 2 mL Luer-Jet Luer-Lock Prefilled Syringe, labeled for intravenous, intramuscular, or subcutaneous use as an opioid antagonist. The carton includes dosing and storage instructions, cautions on proper syringe engagement, and is manufactured by International Medication Systems, Limited. NDC 76329-3369-1 is displayed along with a barcode.*

* 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.