Fosaprepitant Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-972

5 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Fosaprepitant (NDC 63323-972). 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.

FDA Label Image

Structural Formula (Fos04 0007 01)

Structural Formula (Fos04 0007 01)
Chemical structure diagram showing the molecular structures of the active ingredient fosaprepitant, as labeled.*
FDA Label Image

Fresenius Kabi Logo (Fos04 0007 02)

FDA Label Image

Fresenius Kabi Logo (Fos04 0007 03)

Fresenius Kabi Logo (Fos04 0007 03)
Fosaprepitant 150 mg/5 mL lyophilized powder for solution injection vial, labeled for intravenous use. The vial label shows the proprietary name Fosaprepitant, strength, dosage form, and the labeler Fresenius Kabi USA, LLC. The label includes storage and handling instructions and is intended for human prescription drug use.*
FDA Label Image

Vial (Fos04 0007 04)

Vial (Fos04 0007 04)
Label for Fosaprepitant injection powder, lyophilized, 150 mg per vial for intravenous use. The label includes storage instructions refrigerating at 2°C to 8°C and details that each vial contains 150 mg of fosaprepitant. It is a single-dose vial labeled for prescription use only, distributed by Fresenius Kabi USA, LLC, with barcode and lot/expiration fields.*
FDA Label Image

Carton (Fos04 0007 05)

Carton (Fos04 0007 05)
Fosaprepitant for Injection 150 mg per vial lyophilized powder for solution injection. Label includes reconstitution instructions with 5 mL of 0.9% Sodium Chloride, storage conditions, inactive ingredients, and warnings against use with solutions containing divalent cations. Product is manufactured by Fresenius Kabi USA, LLC, with package barcode and NDC 63323-972-10 visible.*

* 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.