Efavirenz, Lamivudine And Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 42385-929

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Efavirenz, Lamivudine And Tenofovir Disoproxil Fumarate (NDC 42385-929). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laurus Labs Limited, 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

Efavirenz-structure (Efavirenz Structure)

Chemical structure diagram depicting the molecular formula of the active ingredients Efavirenz, Lamivudine, and Tenofovir Disoproxil Fumarate in the drug product by Laurus Labs Limited. The structure shows specific atoms and bonds characteristic of these compounds.*

FDA Label Image

Principal Display Panel (Container Label (30's count))

Label for Efavirenz, Lamivudine and Tenofovir Disoproxil Fumarate Tablets showing strengths of 400 mg, 300 mg, and 300 mg respectively. The film-coated oral tablets come in a package of 30 and are manufactured by Laurus Labs Limited for Laurus Generics Inc. Storage and usage cautions are also displayed, along with a pharmacist alert and child-resistant packaging information.*

FDA Label Image

Lamivudine-structure (Lamivudine Structure)

Chemical structure diagram of the active ingredient Efavirenz, Lamivudine and Tenofovir Disoproxil Fumarate, depicting its detailed molecular configuration with various chemical bonds and atoms.*

FDA Label Image

Tenofovir-structure (Tenofovir Structure)

Chemical structure diagram of Tenofovir Disoproxil Fumarate, one of the active ingredients in the Efavirenz, Lamivudine, and Tenofovir Disoproxil Fumarate combination tablet by Laurus Labs Limited.*

* 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.