Naloxone Hydrochloride Injection
Product Images NDC 0641-6132

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 0641-6132). 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure And Formula (Naloxone Hydrochloride Injection Usp 1)

Chemical Structure And Formula (Naloxone Hydrochloride Injection Usp 1)
Chemical structure of naloxone hydrochloride showing its molecular configuration and chemical name as (-)-17-Allyl-4, 5a-epoxy-3, 14-dihydroxymorphinan-6-one hydrochloride.*
FDA Label Image

Ndc 0641-6132-01 Naloxone HCl Injection, Usp 0.4 mg/ml For Iv, Im Or Sc Use Protect From Light 1 mL Vial Rx Only (Naloxone Hydrochloride Injection Usp 2)

Ndc 0641-6132-01 Naloxone HCl Injection, Usp 0.4 mg/ml For Iv, Im Or Sc Use Protect From Light 1 mL Vial Rx Only (Naloxone Hydrochloride Injection Usp 2)
Label for Naloxone Hydrochloride HCl Injection USP, 0.4 mg/mL in a 1 mL vial by Hikma Pharmaceuticals USA Inc. The injection is for intravenous, intramuscular, or subcutaneous use. The label includes protection instructions and indicates the product is prescription only with NDC 0641-6132-01.*
FDA Label Image

Ndc 0641-6132-25 Rx Only Naloxone HCl Injection, Usp 0.4 mg/ml For Intravenous, Intramuscular Or Subcutaneous Use 25 X 1 mL Vials Light Sensitive: Keep Covered In Carton Until Time Of Use. To Open (Cut seal along dotted line. Each mL contains naloxone hydrochloride 0.4 mg, sodium chloride 8.6 mg, methylparaben 1.8 mg and propylparaben 0.2 mg in Water for Injection. pH 3.0-4.5; hydrochloric acid and/or sodium hydroxide used, if needed, for pH adjustment. USUAL DOASGE: See package insert. Store at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature]. Avoid freezing. PROTECT FROM LIGHT: Keep covered in carton until time of use.)

Ndc 0641-6132-25 Rx Only Naloxone HCl Injection, Usp 0.4 mg/ml For Intravenous, Intramuscular Or Subcutaneous Use 25 X 1 mL Vials Light Sensitive: Keep Covered In Carton Until Time Of Use. To Open (Cut seal along dotted line. Each mL contains naloxone hydrochloride 0.4 mg, sodium chloride 8.6 mg, methylparaben 1.8 mg and propylparaben 0.2 mg in Water for Injection. pH 3.0-4.5; hydrochloric acid and/or sodium hydroxide used, if needed, for pH adjustment. USUAL DOASGE: See package insert. Store at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature]. Avoid freezing. PROTECT FROM LIGHT: Keep covered in carton until time of use.)
Naloxone Hydrochloride Injection, USP 0.4 mg/mL vial label for intravenous, intramuscular, or subcutaneous use. The label shows the NDC 0641-6132-25, manufacturer Hikma Pharmaceuticals USA Inc., and storage instructions to keep at 20° to 25°C and protected from light in the carton. It includes details on contents per mL and mentions usual dosage directions on the package insert. The label also displays batch and expiration date fields and a barcode.*
FDA Label Image

Naloxone Hydrochloride Injection Usp 4

Naloxone Hydrochloride Injection Usp 4
A small rectangular label featuring regulatory and tracking information, including a GTIN barcode number, serial number, expiration date placeholder, and lot number code for Naloxone Hydrochloride injection by Hikma Pharmaceuticals USA Inc. The label is black text on a white background with a QR code on the left.*

* 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.