Ondansetron
Product Images NDC 51672-4091

2 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 51672-4091). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Ondansetron 01)

Chemical Structure (Ondansetron 01)
Chemical structure of ondansetron hydrochloride dihydrate, showing the molecular configuration with indicated HCl and 2H2O components.*
FDA Label Image

Principal Display Panel (50 mL Bottle Carton)

Principal Display Panel (50 mL Bottle Carton)
Ondansetron Oral Solution USP, 4 mg/5 mL in a 50 mL package from Sun Pharmaceutical Industries, Inc. The label includes dosage strength and administration storage instructions, barcodes, and manufacturer details by Taro Pharmaceutical Industries Ltd., Israel. The package is marked Rx only, with branding by TARO.*

* 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.