Cefuroxime Axetil
Product Images NDC 67296-0747

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 67296-0747). 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.

Product Images & Figures Index

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 strength. The label indicates a package of 20 tablets and states it is Rx only. It includes storage instructions and manufacturer information for Alkem Laboratories Ltd., India, distributed by Ascend Laboratories, LLC. The label shows the product NDC 67877-215-20 and contains a barcode.*
FDA Label Image

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

Cefuroxime-500-mg-60tab (Cefuroxime 500 mg 60tab)
Label for Cefuroxime Axetil tablets USP 500 mg, showing a package of 60 tablets. The label includes manufacturer information (Alkem Laboratories Ltd., India) and distributor (Ascend Laboratories, LLC). It states storage conditions and prescription-only status. The label features a barcode and the Ascend Laboratories logo.*
FDA Label Image
Cefuroxime-alkem-logo (Cefuroxime Alkem Logo)
FDA Label Image

Cefuroxime-structure (Cefuroxime Structure)

Cefuroxime-structure (Cefuroxime Structure)
Chemical structure diagram of the active ingredient Cefuroxime axetil, showing its molecular bonds and atoms clearly arranged in a structural formula.*

* 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.