Naloxone Hydrochloride Injection, Solution
Product Images NDC 71872-7219

3 FDA label images from Medical Purchasing Solutions, Llc · 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 Naloxone Hydrochloride (NDC 71872-7219). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7219-1.pdp (71872 7219 1)

71872-7219-1.pdp (71872 7219 1)
Label for Naloxone Hydrochloride Injection USP 0.4 mg per mL, single-dose vial. The injection is for intravenous, intramuscular, or subcutaneous use. The label provides directions for aseptic technique and storage at controlled room temperature. It is distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ, and manufactured by a company in India. The vial count is one.*
FDA Label Image

Package Label-principal Display Panel-0.4 mg Per mL (Container Label)

Package Label-principal Display Panel-0.4 mg Per mL (Container Label)
Label for Naloxone Hydrochloride Injection, USP 0.4 mg/mL in a 1 mL single-dose vial. The label indicates use for intravenous, intramuscular, or subcutaneous administration and notes protection from light. Manufactured in India for AuroMedics Pharma LLC by Medical Purchasing Solutions, LLC.*
FDA Label Image

Chemical Structure (Naloxone Str)

Chemical Structure (Naloxone Str)
Chemical structure of Naloxone Hydrochloride showing its molecular framework including hydroxyl groups, an allyl substituent, and morphinan backbone as labeled in the image.*

* 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.