Voriconazole Injection, Powder, Lyophilized, For Solution
Product Images NDC 71288-027

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Voriconazole (NDC 71288-027). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal 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

Structural Formula (Vor01 0003 01 V3)

Chemical structure of voriconazole showing its triazole and fluorinated aromatic rings, with hydroxyl and methyl substituents, consistent with the active ingredient voriconazole.*

FDA Label Image

Meitheal Logo (Vor01 0003 02 V3)

FDA Label Image

Iprincipal Display Panel – Voriconazole For Injection, 200 mg Container Label (Vor01 0003 03 V3)

Label for Voriconazole for Injection 200 mg per vial, an intravenous lyophilized powder for solution by Meitheal Pharmaceuticals Inc. It indicates a single-dose vial for intravenous infusion with storage and dilution instructions, barcodes, lot, and expiration date fields.*

FDA Label Image

Principal Display Panel – Voriconazole For Injection, 200 mg Carton (Vor01 0003 04 V3)

Voriconazole 200 mg for Injection packaging label showing a lyophilized powder for intravenous use. Label displays the strength of 200 mg per vial, with instructions for reconstitution to yield 10 mg/mL concentration. It states single-dose vial and discard unused portion. The labeler is Meitheal Pharmaceuticals Inc., with NDC 71288-027-30 and storage instructions at 15° to 30°C. Contains barcodes and manufacturer information.*

* 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.