Biktarvy Tablet
Product Images NDC 50090-6247

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 Biktarvy (NDC 50090-6247). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Chemical Structure (Biktarvy 01)

Chemical Structure (Biktarvy 01)
Chemical structure of bictegravir sodium, one of the active ingredients in Biktarvy tablets. The diagram shows the molecular arrangement including rings, functional groups, and sodium (Na+) ion.*
FDA Label Image

Chemical Structure (Biktarvy 02)

Chemical Structure (Biktarvy 02)
Chemical structure of bictegravir sodium, the active ingredient in Biktarvy tablets. The structure shows a fluorinated bicyclic compound linked to a sulfur-containing five-membered ring with an alcohol functional group.*
FDA Label Image

Chemical Structure (Biktarvy 03)

Chemical Structure (Biktarvy 03)
Chemical structure of the active ingredients bictegravir sodium, emtricitabine, and tenofovir alafenamide fumarate as presented in the Biktarvy label. The structure includes detailed molecular connectivity and components.*
FDA Label Image

Label Image (Lbl500906247)

Label Image (Lbl500906247)
Biktarvy tablet carton label containing bictegravir sodium, emtricitabine, and tenofovir alafenamide fumarate. The label specifies a strength of 50 mg, 200 mg, and 25 mg per tablet. The box holds 30 tablets and is labeled by A-S Medication Solutions, Libertyville, IL. The NDC number 50090-6247-0 is visible along with storage instructions to store below 86 degrees Fahrenheit.*

* 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.