Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 70518-4145

View Photos of 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 70518-4145). 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)

Remedy_label (Remedy Label)
This is a description of Ondansetron 4 mg tablets with a quantity of 16. The medication is manufactured by Rising Pharma, Inc., located in Allendale, NJ. The packaging includes instructions to protect from light, store at 20-25°C (58-77°F) with excursions permitted to 15-30°C (59-86°F), and keep out of reach of children. The product is available by prescription only with an NDC number provided. The directions for use are indicated to be found in the package insert. Also, it mentions the repackaging information by RemedyRepack Inc. in Indiana, PA.*
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.