Cefuroxime Axetil Tablet, Film Coated
Product Images NDC 80425-0571

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 80425-0571). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, Llc, 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 Axetil 500mg #20 (Cefuroxime Axetil 500mg Tablet 80425 0571 01)

Cefuroxime Axetil 500mg #20 (Cefuroxime Axetil 500mg Tablet 80425 0571 01)
Label for Cefuroxime axetil 500 mg film-coated tablets, 20 count, by Advanced Rx of Tennessee, LLC. The label includes product name, strength, dosage form, NDC 80425-0571, lot, expiration date 12/31/2027, storage instructions, and barcode. Compared to Ceftin, with reference source NDC 67877-0216-60.*
FDA Label Image

Cefuroxime Axetil 500mg #60 (Cefuroxime Axetil 500mg Tablet 80425 0571 02)

Cefuroxime Axetil 500mg #60 (Cefuroxime Axetil 500mg Tablet 80425 0571 02)
Packaged tablet label for Cefuroxime Axetil 500 mg, film coated, oral dosage form. The label indicates 60 tablets supplied by Advanced Rx of Tennessee, LLC. It includes the product NDC 80425-0571 and notes it is for Rx only. Storage instructions specify keeping between 20°C and 25°C. The label also references comparison to Ceftin and provides expiration and lot placeholders.*
FDA Label Image
FDA Label Image

Cefuroxime-structure (Cefuroxime Structure)

Cefuroxime-structure (Cefuroxime Structure)
Chemical structure of the active ingredient cefuroxime axetil, showing its molecular connectivity and key functional groups relevant to its antibiotic properties.*

* 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.