Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 60760-636

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 60760-636). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

Ondansetron 60760 636 10 Updated

Ondansetron Hydrochloride 4 mg film-coated tablets packaging label by St. Mary's Medical Park Pharmacy. The label states quantity of 10 tablets, with placeholders for lot number and expiration date. It includes manufacturer information (Aurobindo Pharma USA, Inc.) and storage instructions to maintain controlled room temperature between 15° and 30°C (59°-86°F). The label reiterates use as directed and Rx only status.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride dihydrate molecule, depicting its fused rings and functional groups as indicated in the diagram.*

* 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.