Emtricitabine And Tenofovir Disoproxil Fumarate
Product Images NDC 67296-1459

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 67296-1459). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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, showing its molecular configuration including amine, fluorine, oxygen, sulfur, and hydroxyl functional groups. The structure depicts the stereochemistry and ring formations relevant to the active ingredient in Emtricitabine and Tenofovir Disoproxil Fumarate.*

FDA Label Image

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Chemical structure of the active ingredient in EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE by Redpharm Drug, Inc., showing the molecular arrangement including nitrogenous bases, phosphate groups, and isopropyl esters along with fumarate as a counterion.*

FDA Label Image

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Label for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets 200 mg/300 mg in a 30-tablet package by Lupin Pharmaceuticals, Inc. It includes dosage information, storage instructions, pharmacy dispensing guidance, a QR code for the medication guide, and the manufacturer Lupin Limited in India. The label displays the NDC 68180-287-06 and emphasizes dispensing with a medication guide.*

FDA Label Image

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Label for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, strength 200 mg/300 mg. The label indicates it contains 100 tablets, with storage instructions and manufacturer details from Lupin Limited, India, and Lupin Pharmaceuticals, Inc., United States. It includes a barcode and a QR code for the medication guide URL.*

* 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.