Structural Formula For Heparin (Heparin 01)
Heparin Sodium Injection, Solution
Product Images NDC 0409-7650
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 0409-7650). 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.
Product Images & Figures Index
Hospira Logo (Heparin 02)
Principal Display Panel (250 mL Bag Label)
This is information on a 250 mL container of Heparin Sodium in 0.45% Sodium Chloride Injection solution. The solution contains 10,000 USP units of Heparin Sodium per 100 mL and may include additives like Sodium Hydroxide and Hydrochloric Acid for pH adjustment. It comes in a single-use container and should not be mixed with other substances. The unused portion should be discarded, and the solution is intended for intravenous use only. It is also mentioned that the container does not contain natural rubber latex, but it contains DEHP.*
Principal Display Panel (250 mL Bag Overwrap)
The text is a set of instructions for opening a container and checking for leaks. The container should not be removed from its overwrap until needed, and leaks should be checked for by squeezing the container after the overwrap has been removed. If leaks are detected, the solution should be discarded as sterility may be compromised. The container should be stored at room temperature and protected from excessive heat and freezing. There is also an insert that provides further information.*
Principal Display Panel (250 mL Bag Label)
This is a description of a Heparin Sodium solution in 0.45% Sodium Chloride Injection. The solution is packaged in a single dose container with a total volume of 50mL. Each mL of the solution contains 50 usP units of Heparin Sodium. The container is for intravenous use only and any unused portion should be discarded. The solution contains additives such as SODIUM HYDROXIDE and/or HYDROCHLORIC.ACID to adjust the pH level. The usual dosage should be seen in the insert provided.*
Principal Display Panel (250 mL Bag Overwrap)
This text appears to be a set of instructions for opening and using a container, likely for a medical or scientific purpose. The container should not be removed from its overwrap until ready for use, and any leaks should be checked for before use. It should be stored at room temperature and protected from excessive heat and freezing. A reference to an insert is also mentioned.*
Principal Display Panel (500 mL Bag Label)
This is a medical product containing Heparin Sodium in 0.45% Sodium Chloride Injection used for intravenous use only. The 100 mL container has a composition of Heparin Sodium of 5000 USP units, sodium chloride of 0.45 g, with EDTA disodium and anhydrous stabilizer added. This product should not have additives, and unused portion needs to be discarded. The manufacturer is Hospira, INC. based in Lake Forest, IL, USA. This product is only available by prescription.*
Principal Display Panel (500 mL Bag Overwrap)
The given text is a set of instructions for opening a container for use. It includes a cautionary statement about not removing the overwrap until ready for use and checking for leaks before using the solution inside. It also provides information about the recommended storage of the container, advising that it be kept at room temperature and protected from heat and freezing. The text refers to an insert for additional information.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
