Triamterene And Hydrochlorothiazide Capsule
Product Images NDC 68382-855

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 Triamterene And Hydrochlorothiazide (NDC 68382-855). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals (usa) 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.

Product Images & Figures Index

FDA Label Image

Image (062dc3f3 09ea 4f21 9435 025c4e9d460b 01)

Image (062dc3f3 09ea 4f21 9435 025c4e9d460b 01)
Chemical structure diagram of the active ingredient Triamterene and Hydrochlorothiazide, showing its molecular framework including sulfonamide, chlorine, and amino groups attached to a bicyclic ring system.*
FDA Label Image

Image (062dc3f3 09ea 4f21 9435 025c4e9d460b 02)

Image (062dc3f3 09ea 4f21 9435 025c4e9d460b 02)
Chemical structure diagram of the active ingredient Triamterene. The diagram shows the molecular framework with nitrogen atoms and amine groups attached to a fused ring system including a benzene ring.*
FDA Label Image

Image (062dc3f3 09ea 4f21 9435 025c4e9d460b 03)

Image (062dc3f3 09ea 4f21 9435 025c4e9d460b 03)
Label for Triamterene and Hydrochlorothiazide Capsules, USP 37.5 mg/25 mg, oral capsules in a 100-count package. The label includes the product name, strengths, a visual of a capsule marked '855', dosage instructions, storage information, manufacturer (Cadila Healthcare Ltd., India), and distributor (Zydus Pharmaceuticals USA Inc., Pennington, NJ). The Zydus Pharmaceuticals logo is displayed.*

* 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.