Hydrochlorothiazide Tablet
Product Images NDC 65862-133

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 65862-133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (25 mg (100 Tablet Bottle))

Package Label-principal Display Panel (25 mg (100 Tablet Bottle))
Label for Hydrochlorothiazide Tablets, USP 25 mg by Aurobindo Pharma Limited. The label shows it is a prescription drug with 100 tablets per container. It includes dosage strength, storage instructions, distribution details by Aurobindo Pharma USA, Inc., and the product is made in India. An over printing and coding area is marked on the label.*
FDA Label Image

Package Label-principal Display Panel (50 mg (100 Tablet Bottle))

Package Label-principal Display Panel (50 mg (100 Tablet Bottle))
Label for Hydrochlorothiazide Tablets, USP 50 mg, a tablet dosage form for further processing. The label indicates 100 tablets per package. It includes storage instructions, distributor information (Aurobindo Pharma USA, Inc.), the NDC number 65862-134-01, and states the product is made in India by Aurobindo Pharma Limited.*
FDA Label Image

Chemical Structure (Hctz Str)

Chemical Structure (Hctz Str)
Chemical structure diagram of Hydrochlorothiazide, showing its molecular formula C7H8ClN3O4S2 and molecular weight 297.74.*

* 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.