Cefpodoxime Proxetil Tablet, Film Coated
Product Images NDC 67296-2347

3 FDA label images from Redpharm Drug · 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 67296-2347). 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

Chemical Structure (Cefpodoxime Str)

Chemical Structure (Cefpodoxime Str)
Chemical structure of cefpodoxime proxetil, depicting the molecular arrangement of the active ingredient used in the oral film-coated tablet form by Redpharm Drug.*
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. The bottle contains 20 tablets and is marked Rx only. Manufactured for Northstar Rx LLC, Memphis, TN, and by Aurobindo Pharma Limited, India. Storage and dispensing instructions are provided along with a barcode and NDC 16714-394-01.*
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, oral film-coated tablets. The package contains 20 tablets. It is labeled Rx only and marked with NDC 16714-395-01. Manufactured by Aurobindo Pharma Limited, India, for Northstar Rx LLC, Memphis, TN. Includes storage instructions and dispensing warnings, as well as a barcode and an over-printing zone.*

* 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.