Ondansetron Hydrochloride Solution
Product Images NDC 0054-0064

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 0054-0064). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Chemical structure of Ondansetron Hydrochloride with two water molecules (dihydrate), showing the molecular arrangement relevant to the active ingredient in the oral solution form.*

FDA Label Image

Ondansetron 50ml Bottle

Label for Ondansetron Oral Solution, USP 4 mg/5 mL, a human prescription drug by Hikma Pharmaceuticals USA Inc. The 50 mL bottle label includes dosage strength, storage instructions to store at controlled room temperature (20° to 25°C), light protection advisories, and a barcode. It specifies that each 5 mL contains 5 mg ondansetron hydrochloride (dihydrate) equivalent to 4 mg ondansetron base.*

* 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.