Hydrochlorothiazide
Product Images NDC 68071-2607

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 68071-2607). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals, 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

Pdp (68071 2607 9)

Pdp (68071 2607 9)
This is a description of NuCare Pharmaceuticals' Hydrochlorothiazide 50mg tablets bottled under the NDC number 68071-2607-09. The bottle contains 90 round light orange to peach break line tablets with an imprint of "H" on one side of the break line and "3" on another side, and the lot number 00000. The tablets contain Hydrochlorothiazide, USP 50mg as the active ingredient. The bottles should be kept out of reach of children and stored within a controlled temperature range of 68-77°F. Consumers should call their doctor if there are any side effects from taking these tablets, and they can also report adverse events to the FDA. The expiration date of the tablets is 00-00.*
FDA Label Image

Structure (Hydrochlorothiazide Str)

* 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.