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Emtricitabine And Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 70771-1709
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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 70771-1709). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Zydus Lifesciences 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.
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This is a description of a medication with the NDC (National Drug Code) number 70774-1621. The medication is in tablet form and contains 153 mg of Emtricitabine, Tenofovir Disoproxil, and Fumarate. The text also includes some errors and characters that do not make sense, making it difficult to understand the full description.*
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This is a product description of Emtricitabine and Tenofovir Disoproxil Fumarate Tablets. The dosage of the tablets is 167 mg/250 mg. The tablets are dispensed separately and come in a pack of 30. The manufacturer is Zydus. The rest of the text is not readable due to errors.*
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Emtricitabine and Tenofovir Disoproxil Fumarate Tablets are a prescription medication used for treating HIV. Each tablet contains 200 mg of emtricitabine and 300 mg of tenofovir disoproxil fumarate. The usual dosage information is included in the package insert. It should be stored between 20°C to 25°C with permitted excursions to 15°C to 30°C. The package is child-resistant and the medication guide is available at the mentioned website or by calling the provided number. This medication is manufactured by Cala Healthcare Ltd in Ahmedabad, India.*
* 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.
