Cefuroxime Sodium Injection, Powder, For Solution
Product Images NDC 25021-119

4 FDA label images from Sagent Pharmaceuticals · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cefuroxime Sodium (NDC 25021-119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Cef0c 0008 01

Cef0c 0008 01
Chemical structure of Cefuroxime sodium depicting the molecular arrangement of the antibiotic compound, including beta-lactam and other chemical groups characteristic of its class.*
FDA Label Image

Cef0c 0008 02

Cef0c 0008 02
A text panel displaying the formula for calculating creatinine clearance (mL/min) differentiated by sex. For males, it shows the formula using weight, age, and serum creatinine levels; for females, the value is adjusted to 0.85 times the male calculation. The panel is part of drug-related clinical information text.*
FDA Label Image

Cef0c 0008 03

Cef0c 0008 03
Label for Cefuroxime sodium injection powder, 1.5 grams per vial, for intravenous use. The single-dose vial contains an equivalent to 1.5 grams of cefuroxime activity. The label includes storage instructions, usage, and manufacturing information by Sagent Pharmaceuticals, Inc., Schaumburg, IL. NDC 25021-119-20 is visible.*
FDA Label Image

Cef0c 0008 04

Cef0c 0008 04
Label for Cefuroxime sodium injection, powder for solution, 750 mg per vial, equivalent to 750 mg of cefuroxime activity. The single-dose vial is for intravenous or intramuscular use. Label includes storage instructions, manufacturer Sagent Pharmaceuticals, and barcodes.*

* 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.