Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 42708-044

2 FDA label images from Qpharma, 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 Hydrochloride (NDC 42708-044). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qpharma, 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

42708 044 05

42708 044 05
Label for Ondansetron Tablets USP, 4 mg, film-coated oral tablets, showing a quantity of 5 tablets. The label includes an NDC number 42708-044-05, distributor QPharma, Inc., and storage instructions to keep at controlled room temperature. It is marked as a sample, not for sale, and Rx only.*
FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical Structure (Ondansetron Str)
Chemical structure of Ondansetron Hydrochloride, displaying its molecular formula with associated hydrochloride and dihydrate components as depicted in the diagram.*

* 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.