Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 43063-986

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 43063-986). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

43063986 Label (43063986)

Packaging label for Losartan Potassium and Hydrochlorothiazide 50 mg/12.5 mg film-coated tablets, containing 30 tablets per bottle. Label shows the NDC 43063-986-30 and is manufactured by PD-Rx Pharmaceuticals, Inc. The label includes dosage strength, lot number E19E13, and expiration date 05/2021. Warnings and reorder information are also visible on the label.*

FDA Label Image

Losartan Chemical Structure (Losartanhctz Str1)

Chemical structure of Losartan Potassium, showing the arrangement of atoms including chlorine, nitrogen, iodine, and potassium components in the molecule.*

FDA Label Image

Hydrochlorothiazide Chemical Structure (Losartanhctz Str2)

Chemical structure of Losartan Potassium and Hydrochlorothiazide active ingredient, showing detailed molecular bonds and groups.*

* 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.