Cefuroxime Axetil Tablet, Film Coated
Product Images NDC 67296-2168

View Photos of 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 Axetil (NDC 67296-2168). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Cefuroxime-250-mg-20tab (Cefuroxime 250 mg 20tab)

Cefuroxime-250-mg-20tab (Cefuroxime 250 mg 20tab)
Label for Cefuroxime axetil tablets, USP, 250 mg film-coated oral tablets in a 20-count package by Ascend Laboratories, LLC. The label includes storage instructions, manufacturer information (Alkem Laboratories Ltd., India), and NDC 67877-215-20. It is marked Rx only and contains barcodes and regulatory codes.*
FDA Label Image

Cefuroxime-500-mg-60tab (Cefuroxime 500 mg 60tab)

Cefuroxime-500-mg-60tab (Cefuroxime 500 mg 60tab)
The label for Cefuroxime Axetil tablets, USP, 500 mg, film-coated oral tablets. The label shows a 60-tablet count, manufactured by Alkem Laboratories Ltd., India, and distributed by Ascend Laboratories, LLC, Parsippany, NJ. The label includes storage instructions and a barcode, with the National Drug Code (NDC) 67877-216-60 clearly visible.*
FDA Label Image
FDA Label Image

Cefuroxime-structure (Cefuroxime Structure)

Cefuroxime-structure (Cefuroxime Structure)
Chemical structure of cefuroxime axetil, the active ingredient in the medication. The diagram shows the molecular arrangement including rings, functional groups, and bonds characteristic to cefuroxime axetil.*

* 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.