Voriconazole Injection, Solution
Product Images NDC 14335-730

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Voriconazole (NDC 14335-730). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hainan Poly Pharm. Co., Ltd., 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

Principal Display Panel (200 mg Vial Carton)

Principal Display Panel (200 mg Vial Carton)
Packaging label for Voriconazole Injection 200 mg per 20 mL (10 mg/mL) intravenous solution by Hainan Poly Pharm. Co., Ltd. The label includes dosage information, storage instructions, and states the product is for intravenous infusion after dilution. The box features the Poly Pharm logo and indicates the product is preservative-free and latex-free.*
FDA Label Image

Principal Display Panel (200 mg Vial Label)

Principal Display Panel (200 mg Vial Label)
Label for Voriconazole Injection 10 mg/mL, with a total of 200 mg per 20 mL single-dose vial. The label shows it is for intravenous infusion, sterile, and contains no natural rubber latex or preservatives. Manufactured by Hainan Poly Pharm. Co., Ltd., China. Storage instructions note keeping it at 2°C to 8°C and protecting from light.*
FDA Label Image

Chemical Structure (Image01)

Chemical Structure (Image01)
Chemical structure of voriconazole, an antifungal agent, depicting its molecular arrangement with fluorinated aromatic rings and triazole groups. The structure corresponds to the active ingredient voriconazole used in 10 mg/mL intravenous injection formulations.*

* 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.