Furosemide Injection, Solution
Product Images NDC 51662-1227

11 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 51662-1227). 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

Vial Label (1000310 0409 6102 19 Furosemide 2ml)

Vial Label (1000310 0409 6102 19 Furosemide 2ml)
Label for Furosemide injection, USP, 10 mg/mL (20 mg/2 mL) solution. The 2 mL vial is labeled for intravenous or intramuscular use. The product is manufactured by Hospira, Inc., Lake Forest, IL, and is marked Rx only with an NDC number 0409-6102-19. The label includes lot and expiration date fields.*
FDA Label Image

Serialized Label (51662 1227 1 Furosemide 2)

Serialized Label (51662 1227 1 Furosemide 2)
Furosemide 20 mg/2 mL injection solution vial, a human prescription drug for intramuscular and intravenous use. The vial has an orange cap and includes a label showing the concentration and distributor information from HF Acquisition Co LLC DBA HealthFirst.*
FDA Label Image

51662122723 Furosemide Pouch Label

51662122723 Furosemide Pouch Label
Label for FUROSEMIDE Injection USP 20 mg/2 mL (10 mg/mL) solution in a 2 mL vial. The label includes NDC 51662-1227-2, lot number 12345, and an expiration date of 2001-03-01. Manufactured by HF Acquisition Co LLC, Mukilteo, WA 98275. The label states use for intravenous or intramuscular injection and storage instructions.*
FDA Label Image

51662122730 Furosemide Case Label

51662122730 Furosemide Case Label
Label for FUROSEMIDE injection, USP 20 mg/2 mL (10 mg/mL) in a 2 mL vial, box of 25, manufactured by HF Acquisition Co LLC, DBA HealthFirst. The label includes the product NDC 51662-1227-3, lot number 12345, and expiration date 2030-01-01. It specifies the route as intravenous or intramuscular injection and storage instructions.*
FDA Label Image

51662122730 Furosemide Rfid Label

51662122730 Furosemide Rfid Label
DataMatrix barcode label containing serialization and expiration information for FUROSEMIDE injection solution by HF Acquisition Co LLC. Text includes serialized identifiers, a reference to the manufacturer's package insert, and states Rx only. Distributed by HF Acquisition Co LLC, Mukilteo, WA.*
FDA Label Image
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table listing various units of sale and concentrations for Furosemide injection, solution. It includes NDCs, packaging details such as carton or bundle quantities, and concentration values (10 mg/mL) with vial or syringe counts. The table distinguishes packaging sizes like 25 vials per carton and 10 syringes per bundle.*
FDA Label Image
FDA Label Image

Serialized Label 51662 1227 1

Serialized Label 51662 1227 1
A label from FUROSEMIDE injection, solution, 10 mg/mL by HF Acquisition Co LLC, DBA HealthFirst, showing lot and serialized data, a barcode, and distribution details including location in Mukilteo, WA. The label indicates prescription use only (RX ONLY) and references the manufacturer's package insert.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of furosemide, showing its molecular arrangement with a benzene ring substituted by chlorine, sulfonamide, carboxylic acid groups, and a furan ring attached via an ether linkage.*
FDA Label Image

Vial Label 51662 1227 1 Updated March 2021

Vial Label 51662 1227 1 Updated March 2021
Label for Furosemide Injection, USP 20 mg/2 mL (10 mg/mL) distributed by Hospira, Inc. The label shows a 2 mL dosage form with NDC 0409-6102-19 and includes space for lot and expiration date information.*

* 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.