Darunavir Tablet, Film Coated
Product Images NDC 72578-147

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Darunavir (NDC 72578-147). 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

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Chemical structure diagram of the active ingredient Darunavir, showing its molecular configuration with various chemical groups and bonds.*
FDA Label Image

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Two side-by-side forest plots comparing GMR (Geometric Mean Ratio) with 90% confidence intervals for Darunavir/ritonavir during the second and third trimesters. The left plot shows twice-daily dosing, and the right shows once-daily dosing. Variables include total and unbound AUC and Cmin, displaying relative pharmacokinetic measures across trimesters.*
FDA Label Image

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Darunavir Tablets 600 mg film-coated tablet label from Viona Pharmaceuticals Inc. The label indicates the package contains 60 tablets and is prescription only. It includes a child-resistant package warning and storage instructions. The label also lists Zydus Lifesciences Ltd. as the manufacturer in Ahmedabad, India, and Viona Pharmaceuticals Inc. as the distributor in Cranford, NJ.*
FDA Label Image

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Darunavir Tablets 800 mg film-coated tablets label showing product name, dosage strength, quantity of 30 tablets, and Rx only designation. The label includes a child-resistant packaging alert and storage instructions. Manufactured by Zydus Lifesciences Ltd and distributed by Viona Pharmaceuticals Inc.*

* 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.