Furosemide Injection, Solution
Product Images NDC 71872-7059

3 FDA label images from Medical Purchasing Solutions, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 71872-7059). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, Llc, 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

Pdp (7059)

Pdp (7059)
Label for Furosemide Injection USP, 20 mg per 2 mL (10 mg per mL) single dose vial. The label indicates intravenous or intramuscular use with storage instructions and usage warnings. Manufactured for Claris Lifesciences Inc., repackaged and distributed by Medical Purchasing Solutions, LLC.*
FDA Label Image

Spl-image-01-structure.jpg (Spl Image 01 Structure)

Spl-image-01-structure.jpg (Spl Image 01 Structure)
Chemical structure of furosemide showing its molecular formula C12H11ClN2O5S and molecular weight 330.74. The diagram displays the arrangement of atoms and functional groups in the furosemide molecule.*
FDA Label Image

Spl-image-05-2ml-25pk.jpg (Spl Image 05 2ml 25pk)

Spl-image-05-2ml-25pk.jpg (Spl Image 05 2ml 25pk)
Label for FUROSEMIDE Injection, USP 20 mg/2 mL (10 mg/mL) solution for injection. The label states it is for intravenous or intramuscular use in a 2 mL single-dose vial. Manufactured for Claris Lifesciences Inc., North Brunswick, NJ. The label includes storage instructions and warnings to discard unused portions and use only if the solution is clear and colorless. The label also displays an NDC barcode and a date of 02/2016.*

* 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.