Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 70518-3511

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 70518-3511). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., 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

Remedy_label (Remedy Label)

This is a description of Ondansetron, an 8 mg tablet available in a quantity of 30. The medication is repackaged by RemedyRepack Inc. and the original manufacturer is Rising Pharma, Inc. It is RX only and the NDC number is 70518-3511-00. The source NDC is 57237-0076-30. It is advised to keep the medication out of the reach of children and store it at 20-25°C (68-77°F). The medication should also be protected from excursions between 15-30°C (59-86°F). For usage instructions, refer to the package insert.*

FDA Label Image

Chemical Structure (Ondansetron Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.