Ondansetron Hydrochloride
Product Images NDC 60760-637

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 60760-637). 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 637 10

Ondansetron Tablets USP 8 mg label showing a 10-count quantity. The label includes the NDC number 60760-637-10 and notes manufacturing by Aurobindo Pharma USA Inc. in East Windsor, NJ, made in India. Additionally, the label states it is packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ, with storage instructions at controlled room temperature of 15°-30°C (59°-86°F). The label also features a barcode and a 2D data matrix code.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride dihydrate, showing its molecular framework including the indole and imidazole rings with associated functional groups and hydrochloride with two water molecules.*

* 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.