Structural Formula Heparin Sodium (Heparin 01)
Heparin Sodium And Dextrose
Product Images NDC 0409-7793
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Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Heparin Sodium And Dextrose (NDC 0409-7793). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hospira, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Structural Formula Dextrose (Heparin 02)
Heparin Sodium And Dextrose Per 100 mL (Heparin 03)
Heparin 04
Heparin 05
This is a single-dose container of Heparin Sodium, with a volume of 250 mL and a concentration of 25,000 usP units/250 mL. It is dissolved in 5% Dextrose injection, placed in a sterile container, and should only be used for intravenous purposes. The sodium metabisulfite present can be dangerous in patients with sensitivity to sulfites. It comes with a warning against adding additives to the solution and is recommended to be used as is, with an unused portion is to be discarded. The solution is distributed by Hospira Inc. and has the NDC number 0409-7793-5. There are instructions for dosage in the prescribing information, and it is not made with natural rubber latex.*
Heparin 06
This is a description of a single-dose container of Heparin Sodium in 5% Dextrose Injection. It contains 100mL of solution, with a strength of 10,000 USP Units/100mL (100 USP Units/mL). The medication is for Rx only and must be administered intravenously, and caution should be taken as it contains sulfites. The solution contains Heparin Sodium, dextrose, citric acid, sodium citrate, and sodium metabisulfite, all in sterile form. The container is not made of natural rubber latex, and any unused portion must be discarded. The usual dosage instructions are provided in the insert, and no other additives should be made to the solution. The manufacturer is Hospira Inc., located in Lake Forest, IL.*
Heparin 07
This is a description of a Heparin Sodium solution that comes in a single-dose container of 100mL. The solution contains heparin sodium 10,000 USP Units, dextrose, hydrous, citric acid, anhydrous, sodium citrate, dihydrate, and sodium metabisulfite. The product is intended for intravenous use and should be stored at 20 to 25°C (68 to 77°F). The packaging contains a warning that the solution contains sulfites. The usual dosage is indicated in the insert, and no additives should be mixed with the solution. The container should be discarded if any portion is unused. Not made with natural rubber latex. The also contains some non-English characters but they are not relevant to the description.*
Heparin 08
This is a single-dose container with 250mL capacity. The container has 12,500 usP units/250 mL HEPARIN. This solution is made of HEPARIN SODIUM IN a 5% DEXTROSE INJECTION. The solution contains SULFITES and is not made with natural rubber latex. The recommended dosage should adhere strictly according to the prescribing information. The container should be discarded once the content exceeds a single pose. This solution is for intravenous use only. The distributor of this product is Hospira, Inc., situated in Lake Forest, IL 60045, USA.*
* 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.
