Vfend Injection, Powder, Lyophilized, For Solution
Product Images NDC 0049-4190

5 FDA label images from Roerig · 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 Vfend (NDC 0049-4190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Roerig, 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

Chemical Structure (Vfend 01)

Chemical Structure (Vfend 01)
Chemical structure of voriconazole, the active ingredient in VFEND injection. The diagram depicts the molecule's arrangement, including triazole and fluorinated aromatic rings, relevant to its antifungal activity.*
FDA Label Image

Logo (Vfend 02)

FDA Label Image

Logo (Vfend 03)

FDA Label Image

Principal Display Panel (200 mg Vial Label)

Principal Display Panel (200 mg Vial Label)
Label for Vfend I.V. (voriconazole) injection, 200 mg vial containing 10 mg/mL of voriconazole as lyophilized powder for solution. The label states it is a sterile single-dose vial for intravenous infusion only, not made with natural rubber latex, and contains no preservatives. Labeled by Roerig under Premier ProRx, made in Ireland, with storage and usage instructions included.*
FDA Label Image

Principal Display Panel (200 mg Vial Carton)

Principal Display Panel (200 mg Vial Carton)
Packaging label for VFEND I.V. (voriconazole) injection, 200 mg lyophilized powder for solution, sterile single-dose vial for intravenous infusion. The label shows storage instructions, dosage and use information, and states it contains no natural rubber latex or preservatives. Distributed by Roerig, a division of Pfizer Inc.*

* 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.