Ondansetron Solution
Product Images NDC 0121-4882

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 0121-4882). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Onda-structure (Ondansetron Os 1)

Chemical structure diagram of Ondansetron hydrochloride dihydrate (HCl·2H2O), the active ingredient shown as a molecular formula with carbon, nitrogen, oxygen atoms, and labeled functional groups.*

FDA Label Image

50 mL (Bottle)

Ondansetron Oral Solution USP 4 mg/5 mL label showing a 50 mL bottle size. The label includes dosage strength, NDC 0121-0882-51, and storage instructions to keep at 20 to 25°C and protect from light. Distributed by PAI Pharma, Greenville, SC, with branding "PAI Pharma" logo and Rx only designation.*

* 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.