Ceftriaxone
Product Images NDC 55648-983

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ceftriaxone (NDC 55648-983). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wockhardt Limited, 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 (37b1b0c4 49ec 4650 A5df 1b448ff26e87 01)

Chemical structure of ceftriaxone showing the detailed molecular arrangement including its beta-lactam ring, thiazine ring, and associated side groups, with sodium salts and hydrate molecules indicated.*

FDA Label Image

Label 250 mg (37b1b0c4 49ec 4650 A5df 1b448ff26e87 02)

Label for Ceftriaxone for Injection, USP, 250 mg per vial by Wockhardt Limited. The vial is for single use only and intended for intramuscular or intravenous use. The label includes the Rx only designation.*

FDA Label Image

Label 500 mg (37b1b0c4 49ec 4650 A5df 1b448ff26e87 03)

Label of Ceftriaxone for Injection, USP 500 mg per vial by Wockhardt Limited. The label indicates it is for prescription use only, single-use vial, suitable for intramuscular or intravenous administration.*

FDA Label Image

Label 1 G (37b1b0c4 49ec 4650 A5df 1b448ff26e87 04)

Label for Ceftriaxone for Injection, USP showing 1 g per vial strength. The label indicates it is a single-use vial for intramuscular or intravenous use, labeled by Wockhardt Limited.*

FDA Label Image

Label 2 G (37b1b0c4 49ec 4650 A5df 1b448ff26e87 05)

Label from a vial of Ceftriaxone for Injection, USP containing 2 grams per vial. The label indicates prescription use only (Rx), single-use vial, and is intended for intramuscular or intravenous administration. The product is labeled by Wockhardt Limited.*

* 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.