Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 31722-535

8 FDA label images from Camber Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Tenofovir Disoproxil Fumarate (NDC 31722-535). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber 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

Tenofovirdisoproxilfumarate300mg1000scountcontainerlabel (Tenofovirdisoproxilfumarate300mg1000scountcontainerlabel)

Tenofovirdisoproxilfumarate300mg1000scountcontainerlabel (Tenofovirdisoproxilfumarate300mg1000scountcontainerlabel)
Label for Tenofovir Disoproxil Fumarate Tablets 300 mg by Camber Pharmaceuticals, Inc. The label indicates 1000 film-coated oral tablets, includes dosage information, storage temperature, and manufacturer details, with barcodes and contact information. Manufactured by Hetero Labs Limited, India, for Camber Pharmaceuticals.*
FDA Label Image

Tenofovirdisoproxilfumarate300mg100scountcontainerlabel (Tenofovirdisoproxilfumarate300mg100scountcontainerlabel)

Tenofovirdisoproxilfumarate300mg100scountcontainerlabel (Tenofovirdisoproxilfumarate300mg100scountcontainerlabel)
Tenofovir Disoproxil Fumarate Tablets 300 mg film-coated tablets packaging label by Camber Pharmaceuticals, Inc. The label indicates a quantity of 100 tablets, includes dosage and storage information, a contact number, and manufacturing details from Hetero Labs Limited, India. It features barcode images and a pink area marked '40 x 35 mm Un varnish Area.'*
FDA Label Image

Tenofovirdisoproxilfumarate300mg30scountcontainerlabel (Tenofovirdisoproxilfumarate300mg30scountcontainerlabel)

Tenofovirdisoproxilfumarate300mg30scountcontainerlabel (Tenofovirdisoproxilfumarate300mg30scountcontainerlabel)
Label for Tenofovir Disoproxil Fumarate Tablets 300 mg by Camber Pharmaceuticals, Inc. The film-coated oral tablet package contains 30 tablets. The label includes dosage strength, NDC 31722-535-30, storage instructions, manufacturer details, and barcodes.*
FDA Label Image

Tenofovirdisoproxilfumarate300mg500scountcontainerlabel (Tenofovirdisoproxilfumarate300mg500scountcontainerlabel)

Tenofovirdisoproxilfumarate300mg500scountcontainerlabel (Tenofovirdisoproxilfumarate300mg500scountcontainerlabel)
Label for Tenofovir Disoproxil Fumarate Tablets, 300 mg, film-coated oral tablets. The label indicates a package size of 500 tablets and is distributed by Camber Pharmaceuticals, Inc. It includes storage instructions, contact information, and manufacturing details by Hetero Labs Limited, India. The label features barcodes and dosage information.*
FDA Label Image

Tenofovirdisoproxilfumarate300mg60scountcontainerlabel (Tenofovirdisoproxilfumarate300mg60scountcontainerlabel)

Tenofovirdisoproxilfumarate300mg60scountcontainerlabel (Tenofovirdisoproxilfumarate300mg60scountcontainerlabel)
Label for Tenofovir Disoproxil Fumarate Tablets 300 mg, film-coated oral tablets supplied in a package of 60 tablets. The label shows the Camber Pharmaceuticals, Inc. logo, the NDC 31722-535-60, and manufacturer information including the Indian manufacturer Hetero Labs Limited. It includes storage instructions and a barcode.*
FDA Label Image

Tenofovirdisoproxilfumaratestructure (Tenofovirdisoproxilfumaratestructure)

Tenofovirdisoproxilfumaratestructure (Tenofovirdisoproxilfumaratestructure)
Chemical structure of Tenofovir Disoproxil Fumarate, showing its molecular composition including the tenofovir disoproxil moiety and fumaric acid component.*
FDA Label Image

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FDA Label Image

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* 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.