Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 42708-059

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 42708-059). 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 059 05

Ondansetron Tablets USP, 8 mg, film-coated oral tablets in a package of 5 tablets by QPharma, Inc. The label indicates sample status, storage at controlled room temperature, and includes blank dosage instructions. The NDC number is 42708-059-05, with lot and expiration dates noted but obscured.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure diagram of Ondansetron Hydrochloride, the active ingredient in this medication, showing its molecular composition and arrangement including the hydrochloride and dihydrate 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.