Vfend Injection, Powder, Lyophilized, For Solution
Product Images NDC 0049-3190

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Vfend (NDC 0049-3190). 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 of the active ingredient in VFEND 10 mg/mL, showing a triazole ring, a substituted aromatic ring with three fluorine atoms, and other functional groups consistent with the antifungal agent voriconazole.*

FDA Label Image

Logo (Vfend 01a)

FDA Label Image

Logo (Vfend 02)

FDA Label Image

Logo (Vfend 02a)

FDA Label Image

Logo (Vfend 03)

FDA Label Image

Principal Display Panel (200 mg Vial Label)

VFEND 10 mg/mL (voriconazole) Injection vial label from Roerig for intravenous infusion. The label states sterile single-dose vial, discard unused portion, and store at controlled room temperature (15°C to 30°C). It prominently notes 'For Intravenous Infusion Only' and contains 200 mg of voriconazole after reconstitution. Distributed by Roerig, a division of Pfizer Inc., New York, NY.*

FDA Label Image

Principal Display Panel (200 mg Vial Carton)

Packaging label for Vfend I.V. (voriconazole) for Injection 200 mg vial, a sterile single-dose vial for intravenous infusion only. The label shows directions for use, storage conditions, the labeler Roerig, and a barcode. The product is noted as Rx only and made in Ireland, 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.