Ondansetron Tablet, Film Coated
Product Images NDC 70518-4245

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 70518-4245). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., 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

Remedy_label (Remedy Label)

Ondansetron 8 mg film-coated tablets packaging label showing a quantity of 30 tablets. The label includes the proprietary name Ondansetron, strength 8 mg, dosage form tablet, and the labeler RemedyRepack Inc. The label also displays NDC number 70518-4245-00 and manufacturer information as Northstar Rx LLC, Memphis, TN.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron, showing the molecular arrangement including a fused indole ring, a ketone group, a methylated nitrogen, and an imidazole ring as part of its hcl dihydrate salt form.*

* 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.