Fosaprepitant Injection, Powder, Lyophilized, For Solution
Product Images NDC 72603-450

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fosaprepitant (NDC 72603-450). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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

Fosaprepitant-carton-label (Fosaprepitant Carton Label)

Fosaprepitant-carton-label (Fosaprepitant Carton Label)
Packaging label for Fosaprepitant for Injection 150 mg per vial, lyophilized powder for solution for intravenous use. The label indicates reconstitution with 5 mL of 0.9% Sodium Chloride for Injection and includes warnings against use with solutions containing divalent cations. Manufactured for Northstar Rx LLC and by MSN Laboratories Private Limited, India. Contains barcode and storage instructions.*
FDA Label Image

Str (Fosaprepitant Structure)

Str (Fosaprepitant Structure)
Chemical structure diagram of Fosaprepitant, showing molecular bonds and functional groups, including fluorine, trifluoromethyl, phosphate, and hydroxyl groups.*
FDA Label Image

Fosaprepitant-vial-label (Fosaprepitant Vial Label)

Fosaprepitant-vial-label (Fosaprepitant Vial Label)
Label for Fosaprepitant for Injection 150 mg per vial, a lyophilized powder for intravenous injection. The single-dose vial is labeled for refrigeration at 2°C to 8°C and indicates unused portions should be discarded. Manufactured for Northstar Rx LLC with manufacturing by MSN Laboratories, India. Includes storage and usage instructions.*

* 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.