Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 87441-064

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 87441-064). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Solutions, 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

Ondansetron 4 mg (8744106401 Ondansetron 4 mg)

Ondansetron Hydrochloride 4 mg film-coated oral tablets label. The label includes the product name Ondansetron Tablets, USP, strength 4 mg, and states Rx only. It includes dosage guidance to refer to the package insert and storage instructions between 20° to 25°C with excursions allowed. The label lists Unit Dose Solutions, Inc. as the repackager and Tuckhoe Enterprises, LLC as the distributor, with their addresses provided. A barcode and spaces for lot number, expiration date, and quantity are also visible.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride dihydrate, showing its molecular arrangement including aromatic rings, nitrogen atoms, and the hydrochloride with two water molecules. The structure is depicted in a standard 2D skeletal formula.*

* 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.