Naloxone Hydrochloride Injection
Product Images NDC 0641-6260

4 FDA label images from Hikma Pharmaceuticals Usa Inc. · 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 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)

Structure (Naloxone Hydrochloride Injection Usp   Remedy Alli 1)
Chemical structure of naloxone hydrochloride showing its molecular framework and associated hydrochloride group, labeled with its full chemical name as (-)-17-Allyl-4, 5α-epoxy-3, 14-dihydroxymorphinan-6-one hydrochloride.*
FDA Label Image

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

462--930-00 (Naloxone Hydrochloride Injection Usp   Remedy Alli 2)
Naloxone Hydrochloride 0.4 mg/mL Injection label for intravenous, intramuscular, or subcutaneous use. The label shows the product name, strength, route of administration, and a note to protect from light. It indicates the vial size is 1 mL and is manufactured by Hikma Pharmaceuticals USA Inc. The label also includes the NDC 0641-6260 and placeholders for lot and expiration dates.*
FDA Label Image

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

462-931-00 (Naloxone Hydrochloride Injection Usp   Remedy Alli 3)
Naloxone Hydrochloride Injection, USP 0.4 mg/mL by Hikma Pharmaceuticals USA Inc. The label specifies the product is for intravenous, intramuscular, or subcutaneous use. It contains 25 single-dose 1 mL vials. The label includes storage instructions, dosing information, and a directive to protect from light. The NDC number 0641-6260-25 is shown alongside manufacturer details.*
FDA Label Image

Layout 1 (Naloxone Hydrochloride Injection Usp Remedy Alli 4)

Layout 1 (Naloxone Hydrochloride Injection Usp   Remedy Alli 4)
A product label for Naloxone Hydrochloride 0.4 mg/mL injection, manufactured by Hikma Pharmaceuticals USA Inc. The label shows traceability information including GTIN, serial number (SN), expiration date (EXP), and lot number (LOT). The label is monochrome and includes a QR code on the left side.*

* 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.