Ondansetron Hydrochloride
Product Images NDC 50436-1880

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 50436-1880). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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 Image (Lbl504360187)

Ondansetron Hydrochloride 4 mg tablet label from Unit Dose Services. The label indicates a package containing 30 tablets. It includes usage warnings such as storage instructions and controlled room temperature. The product is distributed by Aurobindo Pharma USA, Inc., located in East Windsor, NJ, with barcodes and placeholder fields for lot number and expiration date.*

FDA Label Image

Lbl504361880

Ondansetron Hydrochloride 8 mg oral tablets in a bottle containing 30 tablets, with film-coated tablets. The label includes storage instructions to keep the product at controlled room temperature and out of reach of children. Distributed by Aurobindo Pharma USA, Inc., manufactured by Mylan, and packaged by Unit Dose Services, LLC. The label also shows NDC 50436-1880-1, with space for lot number and expiration date, and indicates the product is prescription only (Rx only).*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure diagram of Ondansetron Hydrochloride Dihydrate. The diagram shows the molecular arrangement including a methylated indole ring and a triazole ring, along with the hydrochloride and two water molecules (dihydrate).*

* 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.