Triamterene Hydrochlorothiazide
Product Images NDC 10544-536

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Triamterene Hydrochlorothiazide (NDC 10544-536). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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

Structure 1 (2817a13e 1e33 4429 8eca 78dc1191aa3d 01)

FDA Label Image

Structure 2 (2817a13e 1e33 4429 8eca 78dc1191aa3d 02)

FDA Label Image

Label 37-5-25mg 30ct (Label Tri HCl Tabs 37 5mg 25mg Bpi(10544 536 30) Sandoz(0781 1123 05) Rev0)

This is a description of medication, Triamterene and Hydrochlorothiazide Tablets, USP 37.5mg/26mg, 30 Tablets, with NDC 10544-536-30 and MFG 0781-1123.05. The Lot# is BP0000000xp ot 0000 with Exp Date: 00000000. The medication should be stored at controlled room temperature and should be kept out of the reach of children.*

FDA Label Image

75mg-50mg 30ct (Label Triamterene Hydrochlorothiazide Tabs 75mg 50mg Bpi(10544 080 30) Sandoz(0781 1008 05) Rev1)

This is a description of a medication called Triamterene and Hydrochlorothiazide Tablets, USP 75mg/50mg, containing 30 tablets in each container. The medication is only available by prescription and should be stored in a controlled room temperature of 20-25 degrees Celsius. The tablets should be stored in a tightly sealed and light-resistant container and kept out of reach of children. The package insert should be consulted for dosage information. The medication is manufactured by Sandoz Inc, based in Bridgeton, NJ, and packaged by Blenheim Pharmacal Inc, based in Narih, NY. The lot number and expiration date for each package of tablets are listed.*

* 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.