Heparin Sodium In Sodium Chloride Injection, Solution
Product Images NDC 51662-1578

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Heparin Sodium In Sodium Chloride (NDC 51662-1578). 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

Bag Labeling (Bag Label)

This is a medical product containing Heparin Sodium, Sodium Chioride, Edetate Disodium, Dihydrate, and Water for Injection. It is for intravenous use only and comes in a single-dose container. NDC 63323-517-01 is used in the treatment of certain medical conditions, and the dosage information can be found in the package insert. The container closure is not made with natural rubber latex, and it is sterile, Non-PVC, Non-DEHP. It is essential to avoid excessive heat and protect from freezing. The manufacturer of this product is Fresenius Kabi, and it has been made in Norway.*

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Dosage (Dosage)

This text appears to be a chart or table displaying different recommended doses and methods of administration for a certain medication, possibly related to blood clotting or similar conditions. The methods described include intermittent intravenous injection, intravenous infusion, and continuous administration, with recommended initial doses ranging from 5,000 to 10,000 units depending on the method used. The recommended frequency of administration also varies, with some methods requiring doses every 4 to 6 hours and others being administered continuously for up to 24 hours.*

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3 (Highlight 3)

This is a set of instructions for the use of Intravascular via Extracorporeal equipment in Dialysis. Users are advised to follow the operating directions provided by the manufacturer carefully.*

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Hs1 (Hs 1)

Product Code 077 is sold in units of 24 and contains a strength of 25,000 USP units per 500 mL. Product Code 517074 is also sold in units of 24 and contains a strength of 25,000 USP units per 250 mL. Both products are available in Single Dose freeflex Bags with corresponding NDC codes.*

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Hs2 (Hs 2)

The text describes two different products with their product codes, strengths, and packaging details. The first product comes in a unit of 24 and has a strength of 50 USP units per mL packed in a 500 mL single-dose freeflex® bag. The second product also comes in a unit of 24, has a strength of 100 USP units per mL, and is packed in a 250 mL single-dose freeflex® bag. The NDC codes are given for both products.*

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1 (Highlights 1)

This is a medication dosing guide for two different methods of administering intravenous injections for patients. The first method involves intermittent injections every 4 to 6 hours with an initial dose of 10,000 units and subsequent doses ranging from 5,000 to 10,000 units. The second method is a continuous intravenous infusion with an initial dose of 5,000 units and subsequent dose of 20,000 to reach a maximum of 40,000 units over a period of 24 hours. The guide is based on a 150 lb (68 kg) patient.*

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2 (Highlights 2)

The text appears to be a medical instruction related to a dose of an unspecified medication. It suggests an initial dose of over 150 units per kilogram of body weight and advises adjusting the dose for longer medical procedures. The context of the medication is not specified.*

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Logo (Logo)

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Serialized Labeling (Serialized Labeling)

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Structure (Structure)

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