Hydrochlorothiazide Tablet
Product Images NDC 67296-2280

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 67296-2280). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Hctz Structural Formula (Image 1)

Hctz Structural Formula (Image 1)
Chemical structure of Hydrochlorothiazide, a pharmaceutical compound, showing detailed molecular bonds and functional groups including chlorine, sulfonamide, and nitrogen-containing rings.*
FDA Label Image

1 (Image 2)

1 (Image 2)
Label for Hydrochlorothiazide Tablets, USP 12.5 mg oral tablets, containing 100 tablets per package. The label shows the NDC number 0172-3444-60 and indicates Rx only. The labeler is Teva, with mention of Redpharm Drug as manufacturer. Additional drug facts and manufacturing details are included in small print on the label.*
FDA Label Image

1 (Image 3)

1 (Image 3)
Label for Hydrochlorothiazide Tablets USP, 25 mg, oral tablet, manufactured by Teva Czech Industries. The label shows NDC 0172-2083-60, pack size 100 tablets, and indicates prescription-only status. Storage instructions recommend 20 to 25°C controlled room temperature. Serialization coding area is present.*
FDA Label Image

1 (Image 4)

1 (Image 4)
Label for Hydrochlorothiazide Tablets, USP 50 mg, oral tablet by Redpharm Drug. The label shows NDC 0172-2089-60, package quantity of 100 tablets, and includes dosage instructions, storage conditions, and manufacturer information by Teva Pharmaceuticals. The Teva logo is visible on the bottom right.*

* 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.