Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 55111-155

3 FDA label images from Dr. Reddy's Laboratories Limited · 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 Hydrochloride (NDC 55111-155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Carton3 (Carton3)

Carton3 (Carton3)
Packaging label for Ondansetron Tablets USP 16 mg oral film-coated tablets. The label indicates this is a prescription drug with 100 tablets packaged as 10 blister cards, each containing 10 unit-dose tablets. The product is manufactured by Dr. Reddy's Laboratories Limited, India, and includes storage and handling information along with the NDC 55111-155-78.*
FDA Label Image

Container3 (Container3)

Container3 (Container3)
Packaging label for Ondansetron Tablets, USP 16 mg oral film-coated tablets by Dr. Reddy's Laboratories Limited. The label indicates a package containing 30 tablets with instructions for dosage and storage, including that each tablet contains ondansetron hydrochloride equivalent to 16 mg ondansetron. The label also shows storage conditions, manufacturer location in India, and a barcode.*
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 attached hydrochloride and two 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.