Tenofovir Disoproxil Fumarate Tablet, Film Coated
Product Images NDC 33342-096

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tenofovir Disoproxil Fumarate (NDC 33342-096). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals 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

Tenofovir-disoproxil-fumarate-fig-1 (Tenofovir Disoproxil Fumarate Fig 1)

Chemical structure diagram of tenofovir disoproxil fumarate showing its molecular arrangement with labeled atoms and bonds.*

FDA Label Image

435 (Tenofoovir Container Label)

Tenofovir Disoproxil Fumarate Tablets 300 mg film coated label from Macleods Pharmaceuticals Limited. The label includes drug strength, dosage form, NDC 33342-096-07, quantity of 30 tablets, storage instructions below 30°C (86°F), and dispensing information to provide a patient information leaflet. Manufactured by Macleods Pharma USA and Macleods Pharmaceuticals Ltd., India.*

FDA Label Image

505 (Tenofovir 300mg 30s Pithampur)

Label for Tenofovir Disoproxil Fumarate Tablets 300 mg, film-coated oral tablets. The label states each tablet contains tenofovir disoproxil fumarate 300 mg (equivalent to tenofovir disoproxil 245 mg). The packaging is for 30 tablets and is manufactured by Macleods Pharmaceuticals Limited and Macleods Pharma USA, Inc. It includes storage instructions and dispensing guidance to keep the container tightly closed and dispense only in the original container.*

FDA Label Image

468 (Tenofovir Carton 300mg)

Packaging label for Tenofovir Disoproxil Fumarate Tablets 300 mg by Macleods Pharmaceuticals Limited. The label shows a 30-tablet bottle with instructions for the pharmacist to dispense the patient information leaflet. The label includes the NDC 33342-096-07, barcode, and storage directions to keep below 30°C in the original container.*

* 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.