Metolazone Tablet
Product Images NDC 0185-5050

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metolazone (NDC 0185-5050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

10mg 100tabs

The label for Metolazone Tablets, USP 10 mg by Sandoz Inc shows a white background with blue and yellow text. It specifies the strength as 10 mg, oral tablet form, with 100 tablets in the package. The label includes storage instructions, a barcode, and cautions about not interchanging formulations with similar drugs. The product is labeled for prescription use only and manufactured by Sandoz Inc in Switzerland.*

FDA Label Image

2.5mg 100tabs

Metolazone Tablets USP 2.5 mg oral tablets by Sandoz Inc. The label indicates an Rx-only prescription drug with a package containing 100 tablets. It includes warnings about formulation interchangeability, storage instructions, and legal information. The product is distributed by Sandoz Inc, Princeton, NJ, and is a product of Switzerland.*

FDA Label Image

5mg 100tabs

Metolazone Tablets USP 5 mg oral tablets in a bottle carton. The label states the count of 100 tablets and indicates prescription use only. The product is distributed by Sandoz Inc, with the label showing the NDC number 0185-0055-01 and includes storage and interchangeability warnings.*

FDA Label Image

Chemical Structure

Chemical structure of Metolazone, a diuretic drug. The structure shows a quinazoline core with a sulfonamide group, a chlorine substituent, and methyl groups attached to the ring system, representing the molecular layout of Metolazone.*

* 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.