Truvada
Product Images NDC 52959-969

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Truvada (NDC 52959-969). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company, 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

Principal Display Panel (Representative Bottle Label)

The image shows a drug packaging label for Truvada Tablet, product NDC 52959-969-03, manufactured by GILEAD in Canada. The label includes lot number TVA01ZD, expiration date 06/11, and specifies that the tablets are blue film-coated. It features multiple dosing instructions and container warnings, including prescription restrictions and storage guidance by H.J. Harkins Company, Inc.*

FDA Label Image

Chemical Structure (Truvada 01)

Chemical structure of the active ingredient in Truvada, showing its molecular arrangement including nitrogen, fluorine, oxygen, sulfur atoms, and hydroxyl groups.*

FDA Label Image

Chemical Structure (Truvada 02)

Chemical structure diagram showing the molecular structures of two components, identified as active ingredients in Truvada. The left structure represents a phosphorylated nucleotide analog, and the right structure depicts a small organic acid molecule. The image illustrates the chemical composition of the active ingredients in Truvada.*

FDA Label Image

Symbol (Truvada 03)

Truvada oral tablet blister pack contains ten tablets arranged in two rows of five. Each tablet is oval and white, featured in a clear plastic blister with a foil backing. The label indicates it is manufactured by H.J. Harkins Company, 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.