Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 72789-034

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 72789-034). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789034 Label (72789034)

Ondansetron Hydrochloride USP 4 mg film-coated tablets label by PD-Rx Pharmaceuticals, Inc. The label includes the product name, strength of 4 mg, and indicates a package size of 12 tablets. The label also displays NDC 72789-034-12, GTIN, lot number H20D48, and expiration date 08/2022. The label is bilingual, with dosing instructions in English and Spanish.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride dihydrate, showing fused rings and functional groups consistent with the active ingredient Ondansetron Hydrochloride.*

* 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.