Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 63187-636

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 63187-636). 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

63187-636-06 (Ondansetron Fig1)

This is a description of Ondansetron 4mg tablets manufactured by Aurobindo Pharma Limited in Hyderabad, India. The tablets are oval shaped and film-coated in white to off-white color. The tablets are debossed with ‘¥' on one side and '91' on the other side. Each film-coated tablet contains Ondansetron hydrochloride USP (dihydrate) equivalent to 4 mg of Ondansetron. The tablets come in a pack of 30 and are stored at 20°C-25°C. The medication should be kept away from children. The NDC number for the tablets is 63187-636-30.*

FDA Label Image

Chemical Structure (Ondansetron Str)

* 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.