Ceftriaxone Injection, Powder, For Solution
Product Images NDC 0143-9678

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ceftriaxone (NDC 0143-9678). 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

Chemical Structure (Ceftriaxone For Injection Usp 1)

Chemical structure of ceftriaxone displayed with detailed atomic connectivity, including sodium ions and hydration (3.5 H2O) notation. The schematic highlights the molecular framework typical of this cephalosporin antibiotic.*

FDA Label Image

Plb279-wes.1 (Ceftriaxone For Injection Usp 2)

Ceftriaxone 10 grams Injection, USP, powder for solution vial label for intravenous use. The label indicates it is a pharmacy bulk package and not for direct infusion, manufactured by Hikma Pharmaceuticals USA Inc. The label includes storage instructions and manufacturer information.*

FDA Label Image

Pbx768-wes.1 (Ceftriaxone For Injection Usp 3)

Ceftriaxone 10 grams injection powder for solution carton label by Hikma Pharmaceuticals USA Inc. It is a pharmacy bulk package for intravenous use only, with clear warnings that it is not for direct infusion or dispensing as a unit. The label includes NDC 0143-9678-01 and storage instructions for the sterile powder.*

FDA Label Image

Resized Image 1 (Ceftriaxone For Injection Usp 4)

A medication label for Ceftriaxone injection, powder for solution, 10 g strength, by Hikma Pharmaceuticals USA Inc. The label includes a QR code, GTIN, serial number, expiration date placeholder, and lot number placeholder. It is intended for intravenous use.*

* 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.