Furosemide Injection, Solution
Product Images NDC 51662-1720

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 51662-1720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Structure (51662 1720 Structure)

Chemical structure diagram of furosemide showing its molecular framework with sulfonamide, carboxyl, chloride, and furan ring functional groups.*

FDA Label Image

Vial (51662 1720 1 Vial Label Rfid)

A small white adhesive label with black text and a barcode containing 2D data matrix. It includes GS1 barcode information and states: "See manufacturer's insert. Distributed by HF Acquisition Co., LLC, Mukilteo, WA 98275". The label also shows "Rx Only". No product name or strength is visible on this label.*

FDA Label Image

Vial (51662 1720 1 Label)

Label for Furosemide Injection, USP 10 mg/mL (100 mg/10 mL) single-dose vial for intravenous or intramuscular use. The label includes the manufacturer Camber Pharmaceuticals, NDC 31722-311-10, drug content and warnings, storage instructions, and contact information. The label measures 65 x 25 mm with Pantone colors 158 C, 2736 C, 1805 C, and black.*

FDA Label Image

Box (51662 1720 3 Case Label)

Label for FUROSEMIDE injection USP 100 mg/10 mL (10 mg/mL) in a 10 mL vial, packaged as a case of 25. The label includes NDC 51662-1720-3, lot number, and expiration date 2030-09-19. Distributed by HF Acquisition Co., LLC, Mukilteo, WA. RX only.*

FDA Label Image

Pouch (51662 1720 2 Furosemide Injection Usp 100 mg10ml (10 mgml) 10 mL Vial Pouch Label Image)

Label for FUROSEMIDE Injection, USP 10 mg/mL, 10 mL vial. The label shows the NDC 51662-1720-2, lot number 789210, and expiration date 2030-09-19. Distributed by HF Acquisition Co., LLC, Mukilteo, WA 98275. The label includes usage instructions and a QR code.*

* 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.