Ondansetron Hydrochloride
Product Images NDC 33261-745

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 33261-745). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals 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

Chemical Structure (Ondansetron HCl 4mg 8mg Tab For Aurobindo 1)

Chemical Structure (Ondansetron HCl 4mg 8mg Tab For Aurobindo 1)
Chemical structure diagram of Ondansetron Hydrochloride displaying its molecular framework with a noted component of hydrochloride and dihydrate (HCl·2H2O).*
FDA Label Image

Image Label (Ondansetron HCl 4mg 8mg Tab For Aurobindo 2)

Image Label (Ondansetron HCl 4mg 8mg Tab For Aurobindo 2)
Packaging label for Ondansetron Hydrochloride 4 mg film-coated tablets by Aidarex Pharmaceuticals LLC. The label states 30 tablets per package, with each white oval tablet containing 4 mg ondansetron hydrochloride. Manufactured by Aurobindo Pharma Limited, Hyderabad, India. The label includes NDC 33261-0417-30 and indicates it is a generic for Zofran.*
FDA Label Image

Image Label (Ondansetron HCl 4mg 8mg Tab For Aurobindo 3)

Image Label (Ondansetron HCl 4mg 8mg Tab For Aurobindo 3)
Ondansetron Hydrochloride 8 mg film-coated tablets, packaged as 30 tablets per container. The label shows the active ingredient ondansetron hydrochloride at 8 mg strength. It is a yellow oval tablet with imprint 92 on one side and F on the reverse. The product is distributed by Aidarex Pharmaceuticals LLC and manufactured by Aurobindo Pharma Limited Hyderabad, India.*

* 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.