Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 68071-1742

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 68071-1742). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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

Pdp (68071 1742 3)

NuCare Pharmaceuticals Ondansetron Hydrochloride 8 mg film-coated tablets packaging label. The label indicates a supply of 30 tablets in a prescription drug format, with instructions referencing use and storage at controlled temperatures of 68-77°F. The label includes the NDC 68071-1742-3 and distributor information for Auribindo Pharma USA, Inc.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride, showing its molecular composition including a benzene ring, nitrogen atoms, and methyl groups, along with the hydrochloride and dihydrate components.*

* 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.