Furosemide Tablet
Product Images NDC 67296-2136

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 67296-2136). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

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Chemical structure of furosemide, showing its molecular components including a benzene ring with attached carboxyl, sulfonamide, chlorine, and furanyl groups.*
FDA Label Image

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Label for Furosemide Tablets USP 20 mg, oral tablets, in a package of 100 tablets. The label includes manufacturer information for Rising Pharmaceuticals, Inc. and Graviti Pharmaceuticals Pvt. Ltd. It states dosage details, warnings, and storage instructions. The label features a barcode and the lot number NVZ 45 X 15.*
FDA Label Image

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Label for Furosemide Tablets, USP 40 mg by Rising Pharmaceuticals. The label indicates the dosage strength as 40 mg, package quantity of 100 tablets, and prescription-only status. It includes storage instructions, warnings, and manufacturer information for Rising Pharmaceuticals, Inc. and Graviti Pharmaceuticals Pvt. Ltd.*
FDA Label Image

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Furosemide Tablets, USP 80 mg oral tablets packaging label, containing 100 tablets. The label shows the product is for prescription use only (Rx only) and includes storage instructions and warnings. Manufactured for Rising Pharmaceuticals, Inc., East Brunswick, NJ, and by Graviti Pharmaceuticals Pvt. Ltd., India. The label features a barcode and additional manufacturing details.*

* 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.