Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 72162-2364

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 72162-2364). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 (Lbl721622364)

Ondansetron Tablets, USP 4 mg film-coated tablets label by Bryant Ranch Prepack. The label includes dosage strength 4 mg, quantity 500 tablets, and storage instructions. It states the product is for oral use and repackaged by Bryant Ranch Prepack, Inc., manufactured by Aurobindo Pharma Limited. The label includes barcode, NDC number 72162-2364-5, and safety/storage guidance.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride depicting the molecular arrangement, including a fused ring system, ketone group, methyl substitutions, and a hydrochloride dihydrate moiety.*

* 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.