Cefuroxime Axetil Tablet, Film Coated
Product Images NDC 67296-2265

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cefuroxime Axetil (NDC 67296-2265). 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

Package Label-principal Display Panel (250 mg (20 Tablets Bottle))

Package Label-principal Display Panel (250 mg (20 Tablets Bottle))
Cefuroxime Axetil Tablets, USP 250 mg film-coated tablets in a package containing 20 tablets. The label indicates it is for prescription use only, distributed by Rising Health, LLC, made in India, with storage and handling instructions included. The NDC number 57237-058-20 is shown along with a barcode and printing/coding zones.*
FDA Label Image

Package Label-principal Display Panel (500 mg (20 Tablets Bottle))

Package Label-principal Display Panel (500 mg (20 Tablets Bottle))
Label for Cefuroxime Axetil Tablets, USP 500 mg by Rising Health, LLC. The label includes the product name and strength prominently, with quantity of 20 film-coated tablets. It states the drug is prescription only and provides storage instructions and distributor information. The label also has a barcode and manufacturing details indicating it is made in India.*
FDA Label Image

Chemical Structure (Cefuroxime Str)

Chemical Structure (Cefuroxime Str)
Chemical structure diagram depicting the molecular formula of Cefuroxime Axetil, the active ingredient in the product Cefuroxime Axetil 250 mg film-coated oral tablets by Redpharm Drug.*

* 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.