Ondansetron Solution
Product Images NDC 65162-691

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 65162-691). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal 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

Structure (Ondansetron Oral Solution 1)

Chemical structure of the active ingredient Ondansetron shown as a two-dimensional molecular diagram including its hydrochloride dihydrate form.*

FDA Label Image

1 (Ondansetron Oral Solution 2)

Ondansetron Oral Solution USP 4 mg/5 mL packaging label from Amneal Pharmaceuticals LLC. The carton features the product name and strength prominently, NDC 65162-691-79, and indicates the solution is supplied in a 50 mL bottle. The label includes storage instructions, dosage caution, and safety information, as well as the Amneal logo at the bottom.*

FDA Label Image

1 (Ondansetron Oral Solution 3)

Ondansetron oral solution USP 4 mg/5 mL label from Amneal Pharmaceuticals LLC. The label specifies the active ingredient amount per 5 mL, storage instructions, and product volume of 50 mL. The NDC number 65162-691-79 is visible along with a barcode and manufacturer details.*

* 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.