Furosemide Injection, Solution
Product Images NDC 51662-1336

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 51662-1336). 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.

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Serialized Labeling (1336 1 Serialized Labeling)

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5166213362 Label

5166213362 Label
Furosemide Injection is a medication used for intravenous or intramuscular use. It comes in a 4mL vial, containing 40mg/4mL (10mg/mL). Each vial has an NDC code of 51662-1336-2, a lot number of ABCDEFGHIJKLMNOPQRST, and an expiration date of 2021-06-01. The medication should not be used if the solution appears discolored or contains particulate. It should be stored at a temperature range of 20 to 25C (68 to 77F) and protected from light. Any unused portions of the medication should be discarded. The product is distributed by HF Acquisition Co., LLC, based in Mukilteo, WA. The original manufacturer's NDC code is 0409-6102-18. Please refer to the manufacturer's package insert for detailed information.*
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5166213363 Rfid Label

5166213363 Rfid Label
This appears to be a serial number and various codes for a medical product. The text recommends referring to the manufacturer's package insert and indicates that it is distributed by HF Acquisition Co., LLC in Washington state. The product is only intended for use with a prescription (Rx Only).*
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5166213363 Label

5166213363 Label
This is a description for AV Honzv [T ยป]z Injection, USP with a concentration of 40mg/4mL. It comes in a vial size of 4mL with a box of 25. The National Drug Code (NDC) is 51662-1336-3 and the lot number is ABCDEFGHIJKLMNOPQRST with an expiration date of June 1, 2021. It is intended for intravenous or intramuscular use only, and it should not be used if the solution is discolored or contains particulate. It should be stored at 20 to 25C (68 to 77F), protected from light, and discarded if any unused portion remains. This drug is prescription only and the manufacturer's package insert should be consulted. It was originally made by NDC 0409-6102-18 and distributed by HF Acquisition Co., LLC in Mukilteo, WA 98275.*
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How Supplied (How Supplied)

How Supplied (How Supplied)
The text describes different Units of Sale for a medication, including its Concentration, NDC code, and packaging details such as the number of vials or syringes per carton/bundle. There are multiple variations of the medication available with different concentrations and packaging options.*
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Logo (Logo How Supplied)

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Structure (Structure)

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Vial (Vial Label)

Vial (Vial Label)
This is a description of an injection medication manufactured by Hospira, Inc. The medication is contained in a single-use vial with a volume of 4 mL and is intended for intravenous or intramuscular use only under prescription. The National Drug Code (NDC) for the medication is 0409-6102-18. The medication contains 40 mg/4 mL (10 mg/mL) of Injection, USP RL-4984. The label warns not to use the medication if the solution appears discolored or contains particulate. The Lot/Exp number is not available in the given text.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.