Voriconazole Injection, Powder, Lyophilized, For Solution
Product Images NDC 72843-441

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Voriconazole (NDC 72843-441). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ubi Pharma 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

Vial Carton (Carton)

Voriconazole for Injection 200 mg/vial carton label for a sterile single-dose vial by UBI Pharma Inc. The label states no preservatives, for intravenous infusion only, and includes reconstitution and dosage instructions. The product is distributed by UBI Pharma Inc., made in Taiwan, with an NDC of 72843-441-01.*

FDA Label Image

Vial Label (Container)

Label for Voriconazole for Injection 200 mg/vial by UBI Pharma Inc., a lyophilized powder for intravenous injection. The label indicates no preservatives, sterile single-dose vial, and instructs to discard unused portions. The label includes storage instructions, reconstitution directions with 19 mL water, and administration notes. The product is made in Taiwan.*

FDA Label Image

Chemical Structure (Structure)

Chemical structure of voriconazole, an antifungal agent. The diagram shows the molecular framework with fluorine atoms, a triazole ring, and chiral centers.*

* 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.