Losartan Potassium Tablet, Film Coated
Product Images NDC 72189-096

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 72189-096). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

09630 (72189 0096 30)

Losartan Potassium 50 mg film-coated tablets in a blister pack containing 30 tablets. The label shows the product name, strength, quantity, and the labeler Direct RX. It also includes NDC 72189-096-30 and manufacturing details.*

FDA Label Image

09690 (72189 0096 90)

Losartan Potassium 50 mg film-coated tablets in a package containing 90 tablets. The label includes the generic name Cozaar, identifies the manufacturer as Direct Rx, and lists the National Drug Code 72189-096. The packaging is primarily yellow with black and white text detailing strength and quantity.*

FDA Label Image

09730 (72189 0097 30)

LOSARTAN POTASSIUM 100 mg film-coated tablets in a package labeled with 30 tablets. The label states it is generic for Cozaar and each tablet contains 100 mg of Losartan Potassium. The labeler is Direct Rx, with NDC 72189-097.*

FDA Label Image

09760 (72189 0097 60)

LOSARTAN POTASSIUM 100 mg film-coated tablets box label containing 60 tablets. The label includes the generic name Losartan Potassium and highlights 100 mg strength. Labeler is DIRECT RX with Product NDC 72189-096. The packaging emphasizes the quantity and dosage information prominently in a yellow box on the label.*

FDA Label Image

09790 (72189 0097 90)

LOSARTAN POTASSIUM 100 mg film-coated tablets in a carton labeled with 90 tablets. The label indicates this is a generic for Cozaar, containing 100 mg of Losartan Potassium USP per tablet. The product is labeled by DIRECT RX, with NDC 72189-096. Additional side panel text includes lot number, fill date, and discard date.*

* 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.