Cefuroxime And Dextrose Injection, Solution
Product Images NDC 0264-3114

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Cefuroxime And Dextrose (NDC 0264-3114). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by B. Braun Medical 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 (Cefuroxime For Injection Usp And Dextrose Injectio 1)

FDA Label Image

3114-11 Container Label (Cefuroxime For Injection Usp And Dextrose Injectio 10)

3114-11 Container Label (Cefuroxime For Injection Usp And Dextrose Injectio 10)
This is a pharmaceutical product description for Cefuraxime for Injection USP with Dextrose Injection USP. The container is a 50mL DUPLEX® CONTAINER and requires mixing of both chambers before use. The reconstituted solution contains 1.5 g of Cefuraxime and approximately 145 g of Hydrous Dextrose USP in Water for Injection USP. The approximate osmolality is 290 mOsmolfkg. The product must be stored at 20-25°C (68-77°F) and protected from light until use. The prepared solution should be clear and free from particulate matter and must be used within 24 hours at room temperature or within 7 days if stored under refrigeration. The container is not made with natural rubber latex, PVC or DEHP, and is for Rx only.*
FDA Label Image

Drug Chamber Label (Cefuroxime For Injection Usp And Dextrose Injectio 11)

Drug Chamber Label (Cefuroxime For Injection Usp And Dextrose Injectio 11)
This is a drug chamber which has instructions to peel the foil strip only at the time of use and discard it if it is damaged. It is advised to inspect the drug before reconstitution. The package insert has complete directions for reconstitution and administration.*
FDA Label Image

Chemical Structure (Cefuroxime For Injection Usp And Dextrose Injectio 2)

FDA Label Image

Diagram 1 (Cefuroxime For Injection Usp And Dextrose Injectio 3)

FDA Label Image

Diagram 2 (Cefuroxime For Injection Usp And Dextrose Injectio 4)

FDA Label Image

Diagram 3 (Cefuroxime For Injection Usp And Dextrose Injectio 5)

FDA Label Image

Diagram 4 (Cefuroxime For Injection Usp And Dextrose Injectio 6)

FDA Label Image

Diagram 5 (Cefuroxime For Injection Usp And Dextrose Injectio 7)

FDA Label Image

3112-11 Container Label (Cefuroxime For Injection Usp And Dextrose Injectio 8)

3112-11 Container Label (Cefuroxime For Injection Usp And Dextrose Injectio 8)
This is a description of Cefl 750, which is a medication that comes in a 50mL container. The medication is a sterile, pyrogen-free solution that contains 750mg of ceuroamal. The instructions explain how to activate the chambers of the container, and recommend that the product be used within 7 days of reconstitution. The description provides approximate molarity and storage information. However, the text is not entirely clear, and some parts are not readable.*
FDA Label Image

Drug Chamber Label (Cefuroxime For Injection Usp And Dextrose Injectio 9)

Drug Chamber Label (Cefuroxime For Injection Usp And Dextrose Injectio 9)
This text is a set of instructions for a drug chamber product. It provides precautions to be taken while using the product and advises to discard the chamber if the foil strip is damaged. The user is advised to reconstitute the drug only when ready for use and after visually inspecting it. There is a reference made to a package insert for complete directions for reconstitution and administration.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.