Ondansetron Tablet, Film Coated
Product Images NDC 16714-159

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 16714-159). 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.

Product Images & Figures Index

FDA Label Image

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

Package Label-principal Display Panel (4 mg Blister Carton (10 x 10 Unit-dose))
Ondansetron Tablets, USP 4 mg film-coated oral tablets label. The label indicates a package size of 30 tablets. Manufactured for NorthStar Rx LLC, Memphis, TN, and by Aurobindo Pharma Limited, India. Includes storage instructions, dosage advice to refer to package insert, and a barcode. The label is marked Rx only and dated 03/2021.*
FDA Label Image

Package Label-principal Display Panel (8 mg (500 Tablet Bottle))

Package Label-principal Display Panel (8 mg (500 Tablet Bottle))
Packaging label for Ondansetron Tablets, USP 8 mg, film-coated oral tablets in a 30 tablet count. The label displays the NorthStar Rx LLC branding and states the product is manufactured by Aurobindo Pharma Limited in India. The label includes storage instructions and highlights it is prescription only.*
FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical Structure (Ondansetron Str)
Chemical structure of Ondansetron hydrochloride dihydrate, showing its molecular arrangement with benzene, ketone, and methyl-substituted rings along with a hydrated hydrochloride group.*

* 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.