Fosabelogo (Fosabelogo)
Fosaprepitant Injection, Powder, Lyophilized, For Solution
Product Images NDC 71839-104
5 FDA label images from Be Pharmaceuticals Inc. · 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 71839-104). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Be Pharmaceuticals Inc., 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
Fosacartonlabel (Fosacartonlabel)
Packaging label for Fosaprepitant for Injection 150 mg per vial, a sterile lyophilized powder for intravenous use. Each vial contains 245.3 mg of fosaprepitant dimeglumine equivalent to 150 mg fosaprepitant for infusion when reconstituted with 5 mL 0.9% Sodium Chloride. The label includes usage instructions, storage conditions (2°C to 8°C), warnings against certain diluents, and is distributed by BE Pharmaceuticals Inc., Cary, NC.*
Fosalogo (Fosalogo)
Fosastr (Fosastr)
Chemical structure of fosaprepitant shown in two parts, illustrating the molecular formula with detailed atomic connections, including fluorine, trifluoromethyl groups, and a lyophilized injection form's chemical components.*
Fosaviallabel (Fosaviallabel)
Label for Fosaprepitant for Injection 150 mg per vial, lyophilized powder for intravenous use. The label includes storage instructions, barcode, distributor BE Pharmaceuticals Inc. from Cary, NC, and states the product is made in India. It specifies single-dose vial and disposal of unused portion.*
* 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.
