Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 70518-4145

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 70518-4145). 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 4 mg film-coated tablets label showing quantity of 16 tablets. The label includes barcode, NDC number 70518-4145-00, manufacturer Rising Pharma, Inc., and repackager RemedyRepack Inc. It instructs to protect the product from light, references directions for use on the package insert, and advises storage between 20-25°C with excursions permitted to 15-30°C.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride dihydrate, showing the molecular arrangement including indole and imidazole rings, a ketone group, and associated hydrochloride and water molecules.*

* 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.