Ondansetron Injection
Product Images NDC 65219-323

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 65219-323). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Ond09 0000 01)

Structural Formula (Ond09 0000 01)
Chemical structure of Ondansetron Hydrochloride dihydrate, showing its molecular arrangement including indole and imidazole rings with a hydrochloride and dihydrate component, corresponding to the injection dosage form of Ondansetron 2 mg/mL by Fresenius Kabi USA, LLC.*
FDA Label Image

Fresenius Kabi Logo (Ond09 0000 02)

Fresenius Kabi Logo (Ond09 0000 02)
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Ondansetron Injection, USP – Vial Label)

Package Label (PRINCIPAL DISPLAY – Ondansetron Injection, USP – Vial Label)
Ondansetron Injection, USP 4 mg per 2 mL (2 mg per mL) single-dose vial label. The vial is for intramuscular or intravenous use and is Rx only. Label includes the Fresenius Kabi logo and a barcode with the NDC 65219-323-00.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Ondansetron Injection, USP – Tray Label)

Package Label (PRINCIPAL DISPLAY – Ondansetron Injection, USP – Tray Label)
Ondansetron Injection, USP 4 mg per 2 mL (2 mg per mL) in single-dose vials with 25 vials per package. For intramuscular or intravenous use, preservative-free. Labeler is Fresenius Kabi USA, LLC. The label includes dosage strength, storage instructions, and notes the vial closure is latex-free.*

* 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.