Ondansetron Tablet, Orally Disintegrating
Product Images NDC 16714-200

3 FDA label images from Northstar Rx Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 16714-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

Package Label-principal Display Panel (4 mg Blister Carton (3 x 10 Unit-dose))

Package Label-principal Display Panel (4 mg Blister Carton (3 x 10 Unit-dose))
Packaging label for Ondansetron Orally Disintegrating Tablets USP 4 mg by NorthStar Rx LLC. The label states 30 tablets arranged in 3 blister cards of 10 tablets each. It includes directions for use, storage information, and warnings. The product is manufactured by Aurobindo Pharma Limited, India, and distributed by NorthStar Rx LLC, Memphis, TN.*
FDA Label Image

Package Label-principal Display Panel (8 mg Blister Carton (3 x 10 Unit-dose))

Package Label-principal Display Panel (8 mg Blister Carton (3 x 10 Unit-dose))
Ondansetron Orally Disintegrating Tablets USP 8 mg carton from NorthStar Rx LLC. This packaging contains 30 tablets in 3 blister cards of 10 tablets each. The label includes dosing, storage, and child-resistant packaging information, as well as illustrated administration instructions. Manufactured by Aurobindo Pharma, product of India.*
FDA Label Image

Chemical Structure (Ondansetronod Str)

Chemical Structure (Ondansetronod Str)
Chemical structure of Ondansetron, the active ingredient in the product. The diagram shows the molecular arrangement and bonds of this compound used in the ondansetron tablets.*

* 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.