Furosemide Injection, Solution
Product Images NDC 72572-190

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 72572-190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Carton-4 (Carton 4)

Furosemide Injection, USP 40 mg/4 mL (10 mg/mL) vial packaging label by Civica, Inc. for intravenous or intramuscular use. The carton contains 25 single-dose vials of 4 mL each. The label includes dosage strength, administration route, storage instructions, and a warning to discard unused portions and use only if solution is clear and colorless.*

FDA Label Image

Carton-5 (Carton 5)

Furosemide Injection, USP 40 mg/4 mL (10 mg/mL) intravenous or intramuscular solution. The packaging label indicates 25 single-dose vials of 4 mL each. Distributed by Civica, Inc. and manufactured by Baxter Pharmaceuticals India Private Ltd.*

FDA Label Image

Civica-logo-2 (Civica Logo 2)

FDA Label Image

Container-3 (Container 3)

Label for Furosemide Injection, USP 10 mg/mL solution, dispensed in a 4 mL single dose vial (40 mg total). Suitable for intravenous or intramuscular use. Distributed by Civica, Inc., manufactured by Baxter Pharmaceuticals India Private Ltd. Label includes active ingredient content, usage route, storage instructions, and barcode.*

FDA Label Image

Description-1 (Description 1)

Chemical structure diagram of furosemide showing the molecular formula C12H11ClN2O5S and molecular weight 330.74, with annotated chemical groups and bonds represented.*

* 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.