Furosemide Injection, Solution
Product Images NDC 25021-320

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 25021-320). 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 (Fur0b 0000 01)

Chemical structure of furosemide, showing the molecular formula C12H11ClN2O5S and molecular weight 330.74. The structure includes a chlorinated aromatic ring with carboxylic acid, sulfonamide, and other functional groups.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Fur0b 0000 02)

Label for Furosemide Injection, USP 20 mg per 2 mL (10 mg per mL) by Sagent Pharmaceuticals. This is a 2 mL single-dose vial for intravenous or intramuscular use. The label includes storage instructions, warnings to discard unused solution, and manufacturer details indicating it is made in India for Sagent Pharmaceuticals in Schaumburg, IL.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Fur0b 0000 03)

Label for Furosemide Injection, USP 40 mg per 4 mL (10 mg per mL) solution for injection in a 4 mL single-dose vial. The label states it is for intravenous or intramuscular use, sterile, preservative-free, and nonpyrogenic. It lists inactive ingredients including sodium chloride and sodium hydroxide, and indicates storage conditions. Manufactured for Sagent Pharmaceuticals, Schaumburg, IL, made in India.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Fur0b 0000 04)

Furosemide Injection, USP 100 mg per 10 mL (10 mg per mL) in a 10 mL single-dose vial for intravenous or intramuscular use. The label shows it is sterile, nonpreservative, and manufactured by Sagent Pharmaceuticals. It includes storage and usage instructions along with the NDC 25021-320-10.*

* 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.