Heparin Sodium Injection
Product Images NDC 71872-7351

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 71872-7351). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, Llc., 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

7351.1.pdp (7351.1)

7351.1.pdp (7351.1)
This product is a Sodium Injection manufactured in China for Northstar Rx LLC. It is for intravenous or subcutaneous use and is not for lock flush. The text also mentions the product is to be used by infusion only.*
FDA Label Image

7351.pdp (7351)

7351.pdp (7351)
This text provides information about a Heparin Sodium Injection medication in a 10mL vial. The product is intended for intravenous or subcutaneous use and is derived from Porcine Intestinal Mucosa. Each mL contains heparin sodium 1,000 USP units, sodium chloride 8.6g, and benzyl alcohol 0.01 mL in water for injection. The usual dosage information is available in the package insert. It is advised to store the medication at temperatures between 20° to 25°C (68° to 77°F). The product is described as sterile and non-pyrogenic. The manufacturer is Northstar Fic LLC located in Memphis, TN, and the medication is distributed by Repackaged Medical Purchasing Solutions in Scottsdale, AZ.*
FDA Label Image

Structure Of Heparin Sodium (Hep Structure)

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