Hydrochlorothiazide Tablet
Product Images NDC 71205-751

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 71205-751). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Hctz Structural Formula (Image 1)

FDA Label Image

71205-751-90 (Image 3)

71205-751-90 (Image 3)
This is a description of Hydrochlorothiazide 50mg tablets in a bottle of 90 tablets with a National Drug Code (NDC) of 71205-751-90. The tablets are light orange, round, flat-faced with a beveled edge, and bisected and debossed with "2089" on one side and "TEVA" on the other. The tablets are RX only and each tablet contains 50mg hydrochlorothiazide, USP. The product is manufactured in Czech Republic by Teva Czech Industries s.r.o. Opava-Komarov and is packaged and distributed by Proficient Rx LP, located in Thousand Oaks, CA. The package has a lot number of 00000 with an expiry date of 00/00/00. The product label includes storage temperature and precautions "Store at 20°-25°C (68°-77°F)".*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.