Product Images Furosemide

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Product Label Images

The following 11 images provide visual information about the product associated with Furosemide NDC 51662-1227 by Hf Acquisition Co Llc, Dba Healthfirst, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

VIAL LABEL - 1000310 0409 6102 19 Furosemide 2mL

VIAL LABEL - 1000310 0409 6102 19 Furosemide 2mL

SERIALIZED LABEL - 51662 1227 1 Furosemide 2

SERIALIZED LABEL - 51662 1227 1 Furosemide 2

51662122723 Furosemide POUCH label

51662122723 Furosemide POUCH label

This is a description of Furosemide Injection, which is a solution meant to be used through injection. It is designed for Intravenous or Intramuscular use and is sterile, nonpyrogenic, and needs to be protected from light. The usual dosage should be checked in the insert and should not be used if the solution contains any particles or is discolored. The unused portion should be discarded and needs to be stored at a temperature of about 20 to 25°C (68 to 77°F). RXONLY. The manufacturer suggests that users should look at the package insert for further information. The NDC number is 51662-1227-2, with a lot of 12345 and an expiry date of March 1, 2001. The manufacturing location is Mukilteo, WA 98275.*

51662122730 Furosemide CASE label

51662122730 Furosemide CASE label

Furosemide is a medication available in injection form with a concentration of 20mg/2mL (10mg/mL). The product comes in a flip-top vial and is available in a pack containing 10mg of Furosemide in 1mL of the solution. The product is intended for intravenous or intramuscular use only, and should be protected from light. The stopper of the vial should be cleansed before use with an antiseptic solution. The product is sterile and nonpyrogenic. The manufacturer recommends discarding any unused portion of the drug. The usual dosage for the product is included within the insert. The drug should not be used if the solution is discolored or contains particulate. The product should be stored between 20°C to 25°C. The details for the product are mentioned on the package along with the RXONLY label. The original manufacturer's NDC is 0409-6102-02.*

51662122730 Furosemide RFID label

51662122730 Furosemide RFID label

HS LOGO - How Supplied Logo

HS LOGO - How Supplied Logo

HOW SUPPLIED - How Supplied

HOW SUPPLIED - How Supplied

The given text represents different products in varying concentrations and their packaging details. The products are available in vials and syringes, with concentration levels ranging from 20mg/2mL to 100mg/10mL. Each carton or bundle contains a specific number of vials or syringes.*

LOGO - Logo

LOGO - Logo

Serialized Label 51662 1227 1

Serialized Label 51662 1227 1

STRUCTURE - Structure

STRUCTURE - Structure

Vial Label 51662 1227 1 Updated March 2021

Vial Label 51662 1227 1 Updated March 2021

This is a description of Furosemide injection, a medication distributed by Hospira, Inc in the USA. The medication comes in a 2mL container with a concentration of 20mg/2mL (10mg/mL) and has the NDC code 0409-6102-19. The product code is RL-7536 and it has a lot number of HH-HHH-AA with a manufacturing date of DMMMYYYY.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.