Triamterene And Hydrochlorothiazide Capsule
Product Images NDC 0781-2074

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 Triamterene And Hydrochlorothiazide (NDC 0781-2074). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

37.5mg 25mglabel

37.5mg 25mglabel
Label for Triamterene and Hydrochlorothiazide Capsules, USP 37.5 mg/25 mg, manufactured by Sandoz Inc. The label states the package contains 100 oral capsules and includes storage instructions and a caution to keep out of reach of children. NDC 0781-2074-01 is visible along with a barcode.*
FDA Label Image

50mg 25mglabel

50mg 25mglabel
Label for Triamterene and Hydrochlorothiazide Capsules, USP 50 mg/25 mg, oral dosage form by Sandoz Inc. The label indicates this is a prescription drug containing 100 capsules. It includes storage instructions, a warning to keep out of reach of children, and the product NDC 0781-2715-01 with manufacturer details in Princeton, NJ.*
FDA Label Image

Hctz Chemical Structure

Hctz Chemical Structure
Chemical structure of the active ingredient Triamterene, showing a heterocyclic compound with chlorine, sulfur, nitrogen, and sulfur dioxide functional groups.*
FDA Label Image

Triamterene Chemical Structure

Triamterene Chemical Structure
Chemical structure of Triamterene and Hydrochlorothiazide, showing the molecular composition and arrangement of atoms characteristic of the active ingredients in the oral capsule formulation by Sandoz Inc.*

* 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.