Hydrochlorothiazide Tablet
Product Images NDC 23155-008

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 23155-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet 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

Bf61afcc 295b 4881 96f1 1f524eaa2e1d 01

Bf61afcc 295b 4881 96f1 1f524eaa2e1d 01
Chemical structure diagram of hydrochlorothiazide, showing its molecular arrangement including a benzothiadiazine ring with chloro, sulfonamide, and amino groups.*
FDA Label Image

Bf61afcc 295b 4881 96f1 1f524eaa2e1d 02

FDA Label Image

Bf61afcc 295b 4881 96f1 1f524eaa2e1d 03

Bf61afcc 295b 4881 96f1 1f524eaa2e1d 03
Hydrochlorothiazide Tablets USP 25 mg oral tablets package label by Avet Pharma, containing 100 tablets. The label includes storage instructions and barcode, with prescription use indicated. Labeler is Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.*
FDA Label Image

Bf61afcc 295b 4881 96f1 1f524eaa2e1d 04

Bf61afcc 295b 4881 96f1 1f524eaa2e1d 04
Label for Hydrochlorothiazide Tablets USP 50 mg oral tablets by Avet Pharma, part of Heritage Pharmaceuticals. The label specifies a count of 100 tablets with directions indicating typical dosage of 2 to 4 tablets daily. Storage instructions advise 20° to 25°C (68° to 77°F) with excursions permitted between 15° to 30°C. Dispense in a tight, light-resistant container. Includes manufacturer and barcode details.*

* 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.