Ondansetron Tablet, Film Coated
Product Images NDC 55154-3551

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 55154-3551). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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

Bag Label (Cb02f2d7 31a9 4f12 880e 7ce7d85440d4 00)

Label for ondansetron hydrochloride film-coated tablets, USP 8 mg strength. The label indicates a package of 10 tablets. It includes storage instructions to keep at 20°-25°C (68°-77°F) and notes the product is for prescription use only. The manufacturer is Dr. Reddy's Laboratories Limited, with distribution by Major Pharmaceuticals and Cardinal Health.*

FDA Label Image

Structure (Structure)

Chemical structure of ondansetron hydrochloride dihydrate, showing a fused bicyclic ring system with a methyl-substituted imidazole ring 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.