Atripla
Product Images NDC 53808-0208

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 Atripla (NDC 53808-0208). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Doh Central Pharmacy, 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

Principal Display Panel (30 Tablet Blister Pack)

Principal Display Panel (30 Tablet Blister Pack)
Atripla 600 mg/200 mg/300 mg tablet label indicating a quantity of 30 tablets. The label shows the lot number, expiration date, and states packaging by DOH Central Pharmacy, Tallahassee, FL with a UPC barcode included.*
FDA Label Image

Chemical Structure (Atripla 01)

Chemical Structure (Atripla 01)
Chemical structure of the active ingredient depicted in the image associated with Atripla, showing a fused ring system with halogen substitutions and a cyclopropyl group, likely representing a complex pharmaceutical compound.*
FDA Label Image

Chemical Structure (Atripla 02)

Chemical Structure (Atripla 02)
Chemical structure diagram of the active ingredient shown with fluorine and sulfur atoms, representing a molecular structure typically associated with pharmaceutical compounds, labeled for Atripla by DOH Central Pharmacy.*
FDA Label Image

Chemical Structure (Atripla 03)

Chemical Structure (Atripla 03)
Chemical structure diagram depicting molecular formulas of components associated with the active ingredients in Atripla, a product by DOH CENTRAL PHARMACY. The structure includes complex organic compounds with multiple rings and phosphate groups.*

* 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.