Hydrochlorothiazide
Product Images NDC 68071-3491

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 68071-3491). 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 3491 1)

Pdp (68071 3491 1)
Label for Hydrochlorothiazide 12.5 mg tablets from NuCare Pharmaceuticals, Inc. The label indicates a quantity of 100 tablets, with the NDC 68071-3491-1. Manufacturer details include Actavis Elizabeth LLC in New Jersey. The label includes medication instructions, lot number, expiration date, manufacturer NDC, a barcode, and warnings to keep out of reach of children and to store at controlled temperatures of 68-77°F.*
FDA Label Image

582023b7-figure-01 (Image 1)

582023b7-figure-01 (Image 1)
Chemical structure of Hydrochlorothiazide showing a benzothiadiazine ring with chlorine, sulfonamide, and other characteristic functional groups.*
FDA Label Image

582023b7-figure-02 (Image 2)

582023b7-figure-02 (Image 2)
Hydrochlorothiazide 25 mg oral tablets packaging label from NuCare Pharmaceuticals, Inc. The label features the product name, strength, dosage form, and labeler prominently in black text on a white background with a red and dark navy border. It includes details such as storage information and NDC code 68071-3491.*

* 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.