Hydrochlorothiazide Tablet
Product Images NDC 72789-296

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 72789-296). 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

Molecular Structure (Molecule)

Chemical structure of Hydrochlorothiazide depicted, showing the molecular arrangement including a benzothiadiazine ring system with sulfonamide and other functional groups typical for this active pharmaceutical ingredient.*

FDA Label Image

72789296 Label (72789296)

The packaging label for Hydrochlorothiazide USP 25 mg tablets from PD-Rx Pharmaceuticals, Inc. shows a bottle label with NDC 72789-296-90. The package contains 90 tablets. The label includes dosage strength, manufacturer information, batch lot L22F39, and expiration date 08/2024. The label also features warnings and instructions to keep out of reach of children and to refer to the package insert for dosage and storage.*

* 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.