Fosaprepitant Injection, Powder, Lyophilized, For Solution
Product Images NDC 72205-083

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fosaprepitant (NDC 72205-083). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novadoz 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

Carton-label (Carton Label)

Packaging label for Fosaprepitant for Injection 150 mg per vial, a sterile lyophilized powder for intravenous use. The label instructs reconstitution with 5 mL of 0.9% Sodium Chloride for Injection. It notes storage between 2°C - 8°C and single-dose vial use. Manufactured by MSN Laboratories Private Limited and labeled by Novadoz Pharmaceuticals LLC. Includes NDC 72205-083-01.*

FDA Label Image

Str (Fosaprepitant Structure)

Chemical structure of Fosaprepitant, showing its molecular components including fluorinated aromatic rings, phosphoryl group, and multiple hydroxyl and amine functional groups.*

FDA Label Image

Vial-label (Vial Label)

Label for Fosaprepitant for Injection, 150 mg per vial, a lyophilized powder for intravenous use. The label states single-dose vial with unused portion discarded, storage instructions refrigerated at 2°C to 8°C, and stability of reconstituted solution for 24 hours at or below 25°C. Manufactured by MSN Laboratories Private Limited, Telangana, India, and distributed by Premier ProRx. Includes barcode, lot and expiration placeholders, and coding area measurements.*

* 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.