Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 63187-709

2 FDA label images from Proficient Rx Lp · 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 63187-709). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

63187-709-30 (Ondansetron Fig3)

63187-709-30 (Ondansetron Fig3)
Ondansetron 8 mg film-coated tablets bottle label from Proficient Rx LP. The label states each tablet contains ondansetron hydrochloride equivalent to 8 mg ondansetron. It includes product ID RO070930, manufacturer Aurobindo Pharma Limited, Hyderabad, India, and storage instructions at 20°-25°C (68°-77°F). The label features barcode, QR code, NDC 63187-709-30, and batch details with placeholders for lot and expiration dates.*
FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical Structure (Ondansetron Str)
Chemical structure of Ondansetron Hydrochloride showing the molecular arrangement including a bicyclic ring, a ketone group, and a substituted imidazole ring with associated 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.