Ondansetron Injection, Solution
Product Images NDC 71872-7162

4 FDA label images from Medical Purchasing Solutions, Llc · 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 71872-7162). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

Pdp (71872 7162 1 Pdp)

Pdp (71872 7162 1 Pdp)
Ondansetron Injection, USP 4 mg/2 mL (2 mg/mL) in a 2 mL single-use fliptop vial. The label includes dosage form as injection solution for intramuscular and intravenous use, lot and expiration placeholders, storage instructions (2 to 8°C), and manufacturer information indicating the product is made in India and repackaged by Medical Purchasing Solutions, LLC in Scottsdale, AZ.*
FDA Label Image

Chemical Structure (Ondansetron 01)

Chemical Structure (Ondansetron 01)
Chemical structure of Ondansetron hydrochloride dihydrate, showing the detailed arrangement of atoms and bonds characteristic of the active pharmaceutical ingredient Ondansetron in its hydrochloride salt form with two water molecules of hydration.*
FDA Label Image

Logo (Ondansetron 02)

FDA Label Image

Principal Display Panel (2 mL Vial Label)

Principal Display Panel (2 mL Vial Label)
Ondansetron Injection, USP label for a 2 mL single-dose vial containing 4 mg/2 mL (2 mg/mL) solution. The label includes storage instructions to protect from light and lists Hospira, Inc., Lake Forest, IL, as distributor. Also visible are the NDC 0409-4755-18 and a barcode.*

* 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.