Ondansetron Tablet, Orally Disintegrating
Product Images NDC 68071-3268

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 68071-3268). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals, 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

Pdp (68071 3268 01 G86)

Ondansetron 4 mg orally disintegrating tablets label from NuCare Pharmaceuticals, Inc. The label shows NDC 68071-3268-1 for a #10 count blister pack. It includes the drug name, strength, dosage form (ODT tablets), and warnings about phenylketonurics and storage instructions to keep out of reach of children and store at controlled temperature 68-77°F. Lot number, expiration date, and barcode are also displayed.*

FDA Label Image

Structure-base (Structure Base)

Chemical structure of Ondansetron, showing the molecular arrangement and bonding of its chemical components.*

FDA Label Image

Structure-hcl (Structure HCl)

Chemical structure of Ondansetron hydrochloride dihydrate, showing its molecular configuration with the hydrochloride (HCl) and two water molecules (2H2O) components.*

* 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.