Triamterene And Hydrochlorothiazide Tablet
Product Images NDC 71610-602

4 FDA label images from Aphena Pharma Solutions - Tennessee, Llc · 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 71610-602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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

Figure (41beee6d 31e9 4a4a 80d0 08f33bd51007 01)

Figure (41beee6d 31e9 4a4a 80d0 08f33bd51007 01)
Chemical structure of triamterene, showing its molecular framework including nitrogen atoms and a phenyl ring, corresponding to an active ingredient in the triamterene and hydrochlorothiazide oral tablet product by Aphena Pharma Solutions.*
FDA Label Image

Figure (41beee6d 31e9 4a4a 80d0 08f33bd51007 02)

Figure (41beee6d 31e9 4a4a 80d0 08f33bd51007 02)
Chemical structure of triamterene, showing the arrangement of sulfur dioxide, chlorine, amino groups, and a benzene ring as part of the molecule.*
FDA Label Image

Bottle Label 37.5 mg / 25 mg (71610 0602 60)

Bottle Label 37.5 mg / 25 mg (71610 0602 60)
Triamterene and Hydrochlorothiazide USP 37.5 mg/25 mg tablets label showing package of 90 tablets. The label includes storage instructions to keep between 20-25 degrees Celsius and dispense in a light-resistant container. Manufactured by Cadila Healthcare Ltd and repackaged by Aphena Pharma Solutions - Tennessee, LLC. The package is marked RX Only with NDC 71610-0602-60.*
FDA Label Image

Aphena Pharma Solutions (TN)

* 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.