Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 51655-016

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 51655-016). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 016 27)

Label (51655 016 27)
The text is a product label for Ondansetron tablets, USP, containing 8mg of the drug. There are 12 tablets in the package, with storage instructions to be kept at 20-25°C and protected from light. The drug is a prescription-only medication and should be kept out of reach of children. The label includes information about the lot number and expiration date of the product. The label also notes the manufacturer as Aurobindo Pharma USA, Inc., based in Indianapolis, Indiana.*
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.