Cefoxitin Injection, Powder, For Solution
Product Images NDC 25021-109

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cefoxitin (NDC 25021-109). 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

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Chemical structure of the active ingredient cefoxitin showing its molecular formula with atomic bonds and groups including a beta-lactam ring, a thiazole ring, and the molecular weight labeled as 449.44.*

FDA Label Image

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A section of a drug facts or pharmacokinetics text panel describing dosage or clearance calculations differentiated by male and female patients. The text includes formulas based on weight, age, and serum creatinine values, likely related to dosage adjustment or pharmacokinetic parameters.*

FDA Label Image

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The image shows a Cefoxitin injection label for intravenous use by Sagent Pharmaceuticals. It identifies cefoxitin powder for solution with a strength of 1 gram per vial. The label states it is a sterile, nonpyrogenic, preservative-free, single-dose vial. Additional details include dosage information and storage instructions on a bright yellow background with black and brown text.*

FDA Label Image

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Cefoxitin 2 grams per vial injection powder for solution label. The label states it is for intravenous use only as a single-dose vial. It includes storage instructions and indicates the product is manufactured by Sagent Pharmaceuticals. The label is purple with text describing the sterile, nonpyrogenic nature and preservative-free formulation.*

* 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.