Ondansetron Tablet, Orally Disintegrating
Product Images NDC 68071-5021

2 FDA label images from Nucare Pharmaceuticals,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 68071-5021). 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 5021 3)

Pdp (68071 5021 3)
Label for Ondansetron ODT 4 mg orally disintegrating tablets, package of 30, distributed by Rising Health, LLC Saddle Brook, NJ, and packaged by NuCare Pharmaceuticals, Inc. The label includes the NDC 68071-5021-3 and states Rx Only. Storage instructions specify controlled temperature between 59-86°F and a warning to keep out of reach of children.*
FDA Label Image

Chemical Structure (Ondansetronod Str)

Chemical Structure (Ondansetronod Str)
Chemical structure of Ondansetron, a prescription drug active ingredient shown as a complex heterocyclic organic molecule with aromatic rings, ketone, and methyl substituents.*

* 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.