Emtricitabine And Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 0093-7704

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Emtricitabine And Tenofovir Disoproxil Fumarate (NDC 0093-7704). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Chemical Structure (Image 1)

Chemical structure diagram of Emtricitabine and Tenofovir Disoproxil Fumarate displaying its molecular components, including nitrogen, oxygen, sulfur, and fluorine atoms arranged in the characteristic rings and chains.*

FDA Label Image

Tenofovir Fumurate Chemical Structure (Image 2)

Chemical structure diagram of Emtricitabine and Tenofovir Disoproxil Fumarate, showing molecular components and bonds representing the active ingredients in the medication.*

FDA Label Image

1 (Image 3)

Label for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, 200 mg/300 mg strength, film-coated oral tablets. The label specifies a package of 30 tablets and is manufactured by Teva Pharmaceuticals USA, Inc. The label includes the NDC 0093-7607-56, barcode, and instructions for pharmacists to dispense the Medication Guide. It has a serialization coding area and revision date of 12/2019.*

FDA Label Image

Image 4

Label for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, 200 mg/300 mg film-coated tablets. The label includes the NDC 0093-7704-56, indicates prescription only, and states a package size of 30 tablets. It also notes storage instructions, dispensing guidance, and is branded by Teva Pharmaceuticals USA, 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.