Voriconazole Tablet, Film Coated
Product Images NDC 72578-063

3 FDA label images from Viona Pharmaceuticals Inc · 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 72578-063). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona 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

Image (D9b5c244 Bbad 485c A10c 74b2261f5762 01)

Image (D9b5c244 Bbad 485c A10c 74b2261f5762 01)
Chemical structure of voriconazole showing the molecular arrangement of atoms including nitrogen, fluorine, hydroxyl groups, and methyl group as part of its antifungal compound.*
FDA Label Image

Figure (D9b5c244 Bbad 485c A10c 74b2261f5762 02)

Figure (D9b5c244 Bbad 485c A10c 74b2261f5762 02)
Label for Voriconazole Tablets 50 mg, film coated oral tablets, containing 30 tablets per container. The label shows the NDC 72578-062-06 and notes the dose strength as 50 mg. It is manufactured by Cadila Healthcare Ltd., India, and distributed by Viona Pharmaceuticals Inc. The label includes usual storage instructions and cautions to keep out of reach of children.*
FDA Label Image

Figure (D9b5c244 Bbad 485c A10c 74b2261f5762 03)

Figure (D9b5c244 Bbad 485c A10c 74b2261f5762 03)
Voriconazole Tablets 200 mg film coated oral tablets label with 30 tablets per container. The label features dosing and storage information, warnings to keep out of reach of children, and manufacturing by Cadila Healthcare Ltd., India. Distributed by Viona Pharmaceuticals Inc, Cranford, NJ.*

* 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.