Cefpodoxime Proxetil Tablet, Film Coated
Product Images NDC 67296-2317

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 Cefpodoxime Proxetil (NDC 67296-2317). 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

Package Label-principal Display Panel (100 mg (20 Tablets Bottle))

Package Label-principal Display Panel (100 mg (20 Tablets Bottle))
Label for Cefpodoxime Proxetil Tablets USP 100 mg, film-coated oral tablets, in a package of 20 tablets. The label indicates the product is for prescription use only, manufactured by Aurobindo Pharma Limited, India, for Northstar Rx LLC, Memphis. Storage instructions, dosage reference, and drug safety details are also provided along with a barcode.*
FDA Label Image

Package Label-principal Display Panel (200 mg (20 Tablets Bottle))

Package Label-principal Display Panel (200 mg (20 Tablets Bottle))
Label for Cefpodoxime Proxetil Tablets, USP 200 mg, film-coated oral tablets. The label states a quantity of 20 tablets and includes storage instructions, dosage note, and warnings to keep out of reach of children. It shows the manufacturer as Aurobindo Pharma Limited, India, and the product is labeled for Northstar Rx LLC, Memphis, TN. The label features the NorthStar Rx logo and includes a barcode.*
FDA Label Image

Chemical Structure (Cefpodoxime Str)

Chemical Structure (Cefpodoxime Str)
Chemical structure of the active ingredient cefpodoxime proxetil, showing its molecular arrangement with labeled rings, ester groups, and functional moieties.*

* 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.