Voriconazole Injection, Powder, Lyophilized, For Solution
Product Images NDC 31722-224

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Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Voriconazole (NDC 31722-224). 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

Carton (Carton)

Carton (Carton)
Voriconazole for Injection 200 mg per vial lyophilized powder for solution, labeled for intravenous infusion only. The sterile single-dose vial is manufactured for Camber Pharmaceuticals, Inc. and Aspiro Pharma Limited. The label notes usage instructions, storage temperature of 15°C to 30°C, and absence of natural rubber latex in vial stoppers. The NDC is 31722-224-31.*
FDA Label Image

Vial (Vial)

Vial (Vial)
Label for Voriconazole Injection, 200 mg per vial, lyophilized powder for intravenous infusion. The label includes the NDC 31722-224-31, instructions for reconstitution to 10 mg/mL concentration, storage conditions, and manufacturer information for Camber Pharmaceuticals, Inc. and Aspiro Pharma Limited.*
FDA Label Image
FDA Label Image

Voriconazole-inj-structure (Voriconazole Inj Structure)

Voriconazole-inj-structure (Voriconazole Inj Structure)
Chemical structure of voriconazole, depicting its molecular arrangement with rings, fluorine (F) atoms, nitrogen (N) atoms, a hydroxyl group (OH), and a methyl group (CH3). This is the active ingredient structure for the intravenous lyophilized powder injection form.*

* 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.