Cefpodoxime Proxetil Tablet, Film Coated
Product Images NDC 69043-006

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 69043-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cronus Pharma 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

Package Label-principal Display Panel (100 mg (100 Tablet Bottle))

Package Label-principal Display Panel (100 mg (100 Tablet Bottle))
Packaging label for Cefpodoxime Proxetil Tablets, USP 100 mg, film-coated oral tablets. The label indicates 100 tablets per container, manufactured for Cronus Pharma LLC. It includes dosing storage instructions, safety warnings, and a barcode. The label shows the product is made in India and includes packaging and handling information.*
FDA Label Image

Package Label-principal Display Panel (200 mg (100 Tablet Bottle))

Package Label-principal Display Panel (200 mg (100 Tablet Bottle))
Label for Cefpodoxime Proxetil Tablets USP 200 mg, oral film-coated tablets, in a package of 100 tablets. The label indicates Rx only status and is manufactured for Cronus Pharma LLC. It includes storage instructions and states the product is made in India. NDC code 69043-007-01 is shown along with bar code and revision date 07/2018.*
FDA Label Image

Chemical Structure (Cefpodoxime Str)

Chemical Structure (Cefpodoxime Str)
Chemical structure diagram of the active ingredient cefpodoxime proxetil, showing its molecular connectivity including heterocyclic rings and functional groups.*

* 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.