Fosaprepitant Injection, Powder, Lyophilized, For Solution
Product Images NDC 68001-675

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fosaprepitant (NDC 68001-675). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Caton (Fosaprepitant for Injection 150 mg per vial)

Packaging label for Fosaprepitant for Injection 150 mg per vial, sterile lyophilized powder for intravenous use by BluePoint Laboratories. The label includes NDC 68001-675-25, instructions for reconstitution with 5 mL of 0.9% Sodium Chloride, storage conditions, and a warning against use with solutions containing divalent cations. Manufactured by MSN Laboratories Private Limited in India, the label also shows a barcode and lot/expiry variable data placeholders.*

FDA Label Image

Str (Fosaprepitant Structure)

Chemical structure of Fosaprepitant showing the molecular arrangement of its atoms including functional groups such as phosphate, fluorophenyl, and trifluoromethyl groups, along with a depiction of its hydrate form.*

FDA Label Image

Vial Label- Fosaprepitant For Injection 150mg Per Vial (Fosaprepitant Vial Label)

Label for Fosaprepitant injection 150 mg per vial, lyophilized powder for intravenous use, manufactured by MSN Laboratories for BluePoint Laboratories. The label includes storage instructions to refrigerate at 2°C to 8°C, stability information for the reconstituted solution, and usage directions emphasizing single-dose vial discard. Barcode and revision details are also 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.