Naloxone Hydrochloride Injection
Product Images NDC 0641-6260

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 0641-6260). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., 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

Structure (Naloxone Hydrochloride Injection Usp Remedy Alli 1)

The text contains chemical formulas and names for a substance called Naloxone Hydrochloride. It is difficult to provide more information without additional context.*

FDA Label Image

462--930-00 (Naloxone Hydrochloride Injection Usp Remedy Alli 2)

Naloxone HCl injection is a prescription medication that is given through IV, IM, or SC use. It is packaged in a 1mL vial and should be protected from light. The lot and expiration date is not available.*

FDA Label Image

462-931-00 (Naloxone Hydrochloride Injection Usp Remedy Alli 3)

This is a medication containing naloxone hydrochloride and OXONE intended for intravenous, intramuscular and subcutaneous use. It comes in 25 vials of 1mL each and should be kept at 20 to 25°C (68° to T7°F) to avoid freezing. The typical dosage should be consulted in the package insert. It is light-sensitive, so it should be kept covered in the carton until it is ready for use. The pH adjustment is performed using hydrochloric acid and/or sodium hydroxide. The manufacturer is Remedy Alliance.*

FDA Label Image

Layout 1 (Naloxone Hydrochloride Injection Usp Remedy Alli 4)

This is a product identification label with a GTIN code of 0301234567896, Serial Number (SN) of 1234567890123, an expiration date of MMMYYYY, and a LOT code of ABCDE12345.*

* 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.