Ondansetron Hydrochloride
Product Images NDC 53002-0572

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 53002-0572). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rpk 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

Label Image (Lbl530020572)

Packaging label for Ondansetron Hydrochloride 4mg tablets by RPK Pharmaceuticals, Inc. The label indicates a container of 10 tablets, with instructions to take tablets as directed by a prescriber. The label includes spaces for patient and prescriber names, lot number, expiration date, and National Drug Code (53002-0572). It confirms the product is prescription-only (Rx).*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride Dihydrate, showing the molecular arrangement including a benzene ring, a methyl-substituted nitrogen, and an imidazole ring with hydrochloride and two water molecules (dihydrate).*

* 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.