Heparin Sodium Injection, Solution
Product Images NDC 71872-7364

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 71872-7364). 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

7364.pdp (7364)

7364.pdp (7364)
Heparin Sodium Injection, USP 1000 U 30 mL multi-dose vial label by Medical Purchasing Solutions, LLC. The label states intravenous or subcutaneous use, derived from porcine intestinal mucosa, sterile and nonpyrogenic. Storage recommended at 20° to 25°C. Contains batch and expiration details along with manufacturer info for Sagent Pharmaceuticals, Schaumburg, IL.*
FDA Label Image

7364m.pdp (7364m)

7364m.pdp (7364m)
Label for Heparin Sodium Injection, USP, 30 mL multi-dose vial by Medical Purchasing Solutions, LLC. The label shows strength as 30,000 USP units per 30 mL (equivalent to 1,000 USP units per mL). It includes usage instructions for intravenous or subcutaneous use and storage conditions. The label also indicates this is not for lock flush.*
FDA Label Image

Structure Of Heparin Sodium (Hep00 0025 01)

Structure Of Heparin Sodium (Hep00 0025 01)
Chemical structure diagram showing five monosaccharide units representing Heparin Sodium. The diagram illustrates the molecular components and connections typical of Heparin Sodium's polysaccharide structure.*

* 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.