Bumetanide Injection, Solution
Product Images NDC 25021-321

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bumetanide (NDC 25021-321). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Structural Formula (Bum02 0000 01)

Chemical structure of bumetanide showing a benzene ring with attached groups including carboxyl (COOH), sulfonamide (SO2NH2), ethoxy (OC2H5), and an amine substituent connected to a propyl chain.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Bum02 0000 02)

Bumetanide Injection, USP 0.25 mg/mL solution in a 4 mL single-dose vial for intravenous or intramuscular use. The label lists the active ingredient concentration as 1 mg per 4 mL and includes manufacturer information for Sagent Pharmaceuticals, Schaumburg, IL. The label also mentions benzyl alcohol as a preservative and storage instructions to protect from light and store at 20° to 25°C.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Bum02 0000 03)

Label for Bumetanide Injection, USP, 2.5 mg per 10 mL (0.25 mg per mL) multi-dose vial. The label states it is for intravenous or intramuscular use and contains benzyl alcohol. Manufacturer is Sagent Pharmaceuticals, Schaumburg, IL, with the product made in India. The label includes the NDC 25021-321-10 and storage instructions.*

* 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.