Ondansetron Tablet, Film Coated
Product Images NDC 55154-3551

3 FDA label images from Cardinal Health 107, Llc · 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 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

Structure (Structure)

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.*
FDA Label Image

4mg Bag Label (50aa5f42 2197 43a5 836a 4e0c96209a8b 01)

4mg Bag Label (50aa5f42 2197 43a5 836a 4e0c96209a8b 01)
Ondansetron 4 mg film-coated tablets label showing each tablet contains ondansetron hydrochloride equivalent to 4 mg ondansetron. The package contains 10 tablets, with storage instructions to keep at 20°-25°C. It includes safety warnings, manufacturer details listing Major Pharmaceuticals and distributor Cardinal Health 107, LLC, and specifies prescription use only.*
FDA Label Image

8mg Bag Label (40b3462a 3eba 414d A595 63f462199bd3 00)

8mg Bag Label (40b3462a 3eba 414d A595 63f462199bd3 00)
Packaging label for ondansetron tablets USP 8 mg. The label indicates the product contains film-coated tablets with 8 mg ondansetron hydrochloride equivalent. It is a 10-tablet unit dose package, distributed by Cardinal Health and Major Pharmaceuticals. Storage instructions and warnings for institutional use are included.*

* 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.