Hydrochlorothiazide Tablet
Product Images NDC 16729-184

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 16729-184). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Accord Healthcare 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

12.5mg Label (Hydrochlorothiazide 125mg 100)

Label for Hydrochlorothiazide Tablets USP 12.5 mg oral tablets, containing 100 tablets per container. The product is prescription only (Rx). Manufactured for Accord Healthcare Inc., Durham, NC, and by Intas Pharmaceuticals Limited, India. The label includes storage instructions and the NDC 16729-182-01.*

FDA Label Image

25mg Label (Hydrochlorothiazide 25mg 100)

Label of Hydrochlorothiazide Tablets USP 25 mg, oral tablets in a container of 100 count. The label includes storage instructions, manufacturer information (Accord Healthcare, Inc. and Intas Pharmaceuticals Limited), and states Rx Only. The label features barcodes and a marked varnish free area.*

FDA Label Image

50mg Label (Hydrochlorothiazide 50mg 100)

Label for Hydrochlorothiazide 50 mg oral tablets by Accord Healthcare Inc. The label shows the product name, strength (50 mg), dosage form (tablets USP), prescription-only status, and package size of 100 tablets. Manufacturer details include Intas Pharmaceuticals Limited, India, with storage and safety instructions included.*

FDA Label Image

Structure (Hydrochlorothiazide Str)

Chemical structure of Hydrochlorothiazide, an active ingredient in the product Hydrochlorothiazide tablets by Accord Healthcare Inc.*

* 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.