Ceftriaxone
Product Images NDC 0143-9768

View Photos of 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 Ceftriaxone (NDC 0143-9768). 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

Ceftriaxone Sodium Structural Formula (Ceftriaxone For Injection Pbp 1)

Ceftriaxone Sodium Structural Formula (Ceftriaxone For Injection Pbp 1)
Chemical structure of ceftriaxone sodium, showing its molecular components including a beta-lactam ring, thiazole ring, and sodium salt form with water of hydration represented as 3.5 H2O.*
FDA Label Image

Principal Display Panel (Ceftriaxone For Injection Pbp 2)

Principal Display Panel (Ceftriaxone For Injection Pbp 2)
CefTRIAxone for Injection, USP 10 g vial label by Hikma Pharmaceuticals USA Inc. The label states it contains 10 grams ceftriaxone equivalent, marked as a pharmacy bulk package not for direct infusion, with storage and handling instructions. Manufactured by GlaxoSmithKline in Italy, distributed by West-ward Pharmaceuticals USA.*
FDA Label Image

Principal Display Panel (Ceftriaxone For Injection Pbp 3)

Principal Display Panel (Ceftriaxone For Injection Pbp 3)
Ceftriaxone Injection, USP 10 g bulk package label from Hikma Pharmaceuticals USA Inc. The label indicates the product is a 10 g pharmacy bulk package containing sterile ceftriaxone sodium for reconstitution. It includes instructions, lot, expiration date fields, and storage information.*

* 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.