Emtricitabine And Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 68180-287

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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 68180-287). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

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Chemical structure of emtricitabine, one of the active ingredients in EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE tablets. The diagram depicts the molecular arrangement including nitrogen, oxygen, fluorine, sulfur atoms, and associated bonds.*
FDA Label Image

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Chemical structure diagram of emtricitabine and tenofovir disoproxil fumarate, representing the molecular arrangement of this active pharmaceutical ingredient combination used in oral tablets.*
FDA Label Image

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Goa Label (F5e749bb 4a50 4b65 Aafd 04fb43447b54 03)
Label for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, 200 mg/300 mg strength, film-coated oral tablets. The label includes the NDC 68180-287-06, directions for pharmacist dispensing with medication guide, storage instructions, manufacturer Lupin Pharmaceuticals, Inc., and a package count of 30 tablets. A QR code and barcode are also visible.*
FDA Label Image

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Emtricitabine and Tenofovir Disoproxil Fumarate Tablets 200 mg/300 mg film-coated oral tablets by Lupin Pharmaceuticals, Inc. The label shows a package containing 100 tablets with the NDC 68180-287-01. It includes storage instructions, manufacturer information, and a QR code linking to the medication guide.*

* 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.