Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 57237-076

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 57237-076). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

Package Label-principal Display Panel (4 mg (30 Tablet Bottle))

Package Label-principal Display Panel (4 mg (30 Tablet Bottle))
This is a description for Ondansetron hydrochloride USP tablets. Each film-coated tablet contains 4 mg of ondansetron hydrochloride dihydrate. The tablets are distributed by Rising Health, LLC and come in a container defined by the USP. The recommended mode of administration is available for dosage and administration. The tablets should be stored at 20° to 25°C (68° to 77°F) with excursions that are permitted to 15°-30°C (59-86°F). The text also includes a code- TS/IDRUGS/19/1993 and a National Drug Code (NDC) 57237 075 30.*
FDA Label Image

Package Label-principal Display Panel (8 mg (30 Tablet Bottle))

Package Label-principal Display Panel (8 mg (30 Tablet Bottle))
This is a medication from Rising Health LLC called Ondansetron. It is a tablet medication that comes in a package with 30 tablets. The usual dosage instructions can be found on the package. It should be kept in a light-resistant container at controlled room temperatures. This medication should be protected from light.*
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.