Cefuroxime Axetil Tablet, Film Coated
Product Images NDC 60687-283

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 60687-283). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp27294

Ahp27294
Blue, oval-shaped film-coated tablet with imprint '204' on one side and a smooth blank reverse side. The tablet is identified as Cefuroxime axetil oral tablet, commonly available in 250 mg and 500 mg strengths, manufactured by American Health Packaging.*
FDA Label Image

Blister

Blister
Multiple identical packaging labels for Cefuroxime Axetil 250 mg film-coated tablets by American Health Packaging. Each label includes the drug name, strength, dosage form, barcodes, lot number, expiration date placeholders, and manufacturer location in Columbus, Ohio. The labels are arranged in a sheet format.*
FDA Label Image

Carton

Carton
Cefuroxime axetil 250 mg film-coated tablets label showing a package of 20 tablets (2 x 10). The label includes the NDC number 60687-272-94, storage instructions (20° to 25°C), dosage caution, and manufacturing details by Alkem Laboratories Ltd., India, with distribution by American Health Packaging, Columbus, Ohio.*
FDA Label Image

Structure

Structure
Chemical structure of cefuroxime axetil, the active ingredient in the product. The diagram illustrates the molecular connections and functional groups typical for this beta-lactam antibiotic prodrug.*

* 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.