Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 0093-7367

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 0093-7367). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Image 1

Chemical structure diagram of Losartan Potassium, showing the molecular structure including a chlorinated pyrimidine ring and a potassium ion (K+). This corresponds to one of the active ingredients in Losartan Potassium and Hydrochlorothiazide tablets.*

FDA Label Image

Image 2

Chemical structure diagram depicting a compound with a benzene ring substituted with chlorine, sulfonamide, and a bicyclic sulfonamide structure. The image corresponds to a chemical structure related to the product Losartan Potassium and Hydrochlorothiazide.*

FDA Label Image

Image 3

Label for Losartan Potassium and Hydrochlorothiazide Tablets USP, 50 mg/12.5 mg, film-coated oral tablets by Teva Pharmaceuticals USA, Inc. The label states the product contains 30 tablets, for prescription use only, and includes storage and usage instructions alongside barcodes and serialization coding area.*

FDA Label Image

Image 4

Label for Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg, film-coated tablets supplied by Teva Pharmaceuticals USA, Inc. The label shows NDC 0093-7369-56 with a quantity of 30 tablets. Dosage instructions and storage conditions are noted, along with standard drug safety and handling warnings.*

FDA Label Image

Image 5

Label for Losartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/25 mg, film-coated tablets. The label shows an NDC number 0093-7368-56 and indicates a package size of 30 tablets. It is a prescription-only oral medication manufactured by Teva Pharmaceuticals USA, Inc. The label includes storage and safety instructions and a serialization coding area.*

* 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.