Ceftriaxone Sodium Injection, Powder, For Solution
Product Images NDC 70518-2499

3 FDA label images from Remedyrepack Inc. · 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 Sodium (NDC 70518-2499). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Ceftriaxone-chemical-structure (Ceftriaxone Vial Hospira 01)

Ceftriaxone-chemical-structure (Ceftriaxone Vial Hospira 01)
Chemical structure diagram of Ceftriaxone Sodium, illustrating its molecular composition with labeled atoms and bonds, including sodium ions and water of hydration.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Ceftriaxone Sodium 1 g injection powder for solution in a single-dose vial. The label indicates a quantity of 10 vials for intramuscular (I.M.) or intravenous (I.V.) use. The product is repackaged by RemedyRepack Inc. and originally manufactured by Hospira, Inc. Additional label details include storage instructions and a QR code.*
FDA Label Image

Mm2 (Ceftriaxone 1g 70518 2499 01)

Mm2 (Ceftriaxone 1g 70518 2499 01)
Label for cefTRIAXone 1 g injection powder for solution, a single-dose vial for intramuscular or intravenous use. The label shows the quantity as 1 vial and states it is repackaged by RemedyRepack Inc. It includes an NDC number (70518-2499-01), manufacturer information (Hospira, Inc.), and directions to see the package insert. The label cautions to keep the medication out of reach of children.*

* 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.