Bumetanide Tablet
Product Images NDC 51672-4225

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Bumetanide (NDC 51672-4225). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Bumetanide 01)

Chemical structure diagram of bumetanide showing its molecular arrangement including carboxyl (COOH), sulfonamide (SO2NH2), and other functional groups attached to a benzene ring.*

FDA Label Image

Principal Display Panel (0.5 mg Tablet Bottle Label)

Bumetanide 0.5 mg oral tablets label from Sun Pharmaceutical Industries, Inc. The label includes the NDC 51672-4223-1 and indicates a package of 100 tablets. It states the active ingredient amount per tablet, manufacturer details, storage instructions, and a barcode.*

FDA Label Image

Principal Display Panel (1 mg Tablet Bottle Label)

Bumetanide 1 mg tablets label showing product name, strength, and dosage form. The label states the package contains 100 tablets and includes storage instructions, manufacturer Taro Pharmaceutical Industries Ltd., and distributor Taro Pharmaceuticals U.S.A., Inc. It features a barcode and warnings to keep medication out of reach of children and prescription only status.*

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Bumetanide Tablets, USP 2 mg oral tablets packaging label from Taro Pharmaceutical Industries Ltd., distributed by Taro Pharmaceuticals U.S.A., Inc. The label indicates a bottle of 100 tablets, specifies storage instructions, and includes cautionary statements and prescribing information notes.*

* 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.