Triamterene And Hydrochlorothiazide Capsule
Product Images NDC 71335-0504

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Triamterene And Hydrochlorothiazide (NDC 71335-0504). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Label Image (Lbl713350504)

This label for Triamterene and Hydrochlorothiazide Capsules, USP, displays the strength as 37.5 mg/25 mg. It indicates the oral dosage form and a package count of 100 tablets. The label includes manufacturer information for Lambert Company, Inc., and repackager Bryant Ranch Prepack, Inc., with barcode and NDC 63629-1507-01. Storage instructions and safety warnings are also present.*

FDA Label Image

Lbl7133505042

Triamterene and Hydrochlorothiazide 37.5 mg/25 mg capsule label from Bryant Ranch Prepack. The label notes comparison to Dyazide 37.5/25 mg capsules by Lannett Company Inc. It includes lot number 1523487, storage instructions at 20°-25°C (68°-77°F), and a notice to keep out of reach of children. The label indicates prescription use only with package quantity of 100 capsules.*

FDA Label Image

Hctz-molec-struc (Triamterene And Hydrochlorothiazide Capsules Usp 1)

Chemical structure of the active ingredient Triamterene. The diagram depicts a fused ring system with sulfonamide groups, chlorine substitution, and nitrogen atoms indicative of its molecular framework.*

FDA Label Image

Triamterene-molec-struc (Triamterene And Hydrochlorothiazide Capsules Usp 2)

Chemical structure diagram of the active ingredient Triamterene, showing its molecular arrangement with labeled atoms and bonds.*

* 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.