Emtricitabine And Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 65862-354

View Photos of 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 65862-354). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (200 mg/300 mg (30 Tablet Bottle))

Package Label-principal Display Panel (200 mg/300 mg (30 Tablet Bottle))
Label for Emtricitabine and Tenofovir Disoproxil Fumarate tablets, 200 mg/300 mg strength, film-coated, containing 30 tablets per package. The label includes the NDC 65862-354, distributor information for Aurobindo Pharma USA, Inc., and storage instructions. It also notes that the product is made in India and provides dispensing guidance for pharmacists.*
FDA Label Image

Chemical Structure-1 (Emtriteno Str1)

Chemical Structure-1 (Emtriteno Str1)
Chemical structure of Emtricitabine, part of the combined drug Emtricitabine and Tenofovir Disoproxil Fumarate in tablet form by Aurobindo Pharma Limited. The diagram depicts atomic arrangements including nitrogen, oxygen, sulfur, fluorine, and carbon atoms characteristic of Emtricitabine's molecular structure.*
FDA Label Image

Chemical Structure-2 (Emtriteno Str2)

Chemical Structure-2 (Emtriteno Str2)
Chemical structure depicting the active ingredients Emtricitabine and Tenofovir Disoproxil Fumarate, showing their molecular components and bonds as part of the product labeled by Aurobindo Pharma 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.