Emtricitabine And Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 42385-953

3 FDA label images from Laurus Labs Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Emtricitabine And Tenofovir Disoproxil Fumarate (NDC 42385-953). 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

Emtricitabine Structure (Emtricitabine Structure)

Emtricitabine Structure (Emtricitabine Structure)
Chemical structure of Emtricitabine, one of the active ingredients in Emtricitabine and Tenofovir Disoproxil Fumarate tablets by Laurus Labs Limited.*
FDA Label Image

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

Principal Display Panel (Container Label (30's count))
Label for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, 200 mg/300 mg, film-coated oral tablets. The label indicates a package containing 30 tablets, manufactured by Laurus Labs Limited and labeled for Laurus Generics Inc. Storage instructions specify 20 to 25°C with permitted excursions. The label includes directions to dispense the accompanying Medication Guide and is marked Rx Only with a visible barcode.*
FDA Label Image

Tenofovir Disoproxil Fumarate Structure (Tenofovir Df Structure)

Tenofovir Disoproxil Fumarate Structure (Tenofovir Df Structure)
Chemical structure of Emtricitabine and Tenofovir Disoproxil Fumarate, showing the molecular arrangement of the active ingredients in the combined pharmaceutical product 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.