Fosaprepitant Injection, Powder, Lyophilized, For Solution
Product Images NDC 31722-165

5 FDA label images from Camber 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 31722-165). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber 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.

FDA Label Image
FDA Label Image
FDA Label Image

Fosaprepinjcarton (Fosaprepinjcarton)

Fosaprepinjcarton (Fosaprepinjcarton)
Box label for Fosaprepitant for Injection 150 mg per vial, a sterile lyophilized powder for intravenous use from Camber Pharmaceuticals, Inc. The label includes reconstitution instructions with 5 mL of 0.9% Sodium Chloride, storage conditions (2°C to 8°C), inactive ingredients, and contact information. Manufactured by Aspiro Pharma Limited in India. The label states the product is for single-dose use and warns against use with solutions containing divalent cations.*
FDA Label Image

Fosaprepinjlabel (Fosaprepinjlabel)

Fosaprepinjlabel (Fosaprepinjlabel)
Label for Fosaprepitant for Injection 150 mg per vial, a lyophilized powder for intravenous use. The single-dose vial is labeled for refrigeration at 2°C to 8°C and displays storage and handling instructions. Manufactured for Camber Pharmaceuticals, Inc. and by Aspiro Pharma Limited in India. The label includes barcode and regulatory information.*
FDA Label Image

Structure.jpg (Structure)

Structure.jpg (Structure)
Chemical structure of Fosaprepitant dimeglumine, the active ingredient in Fosaprepitant injection powder.*

* 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.