Heparin Sodium Injection
Product Images NDC 71872-7352

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 71872-7352). 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

7352.1.pdp (7352.1)

7352.1.pdp (7352.1)
Label for Heparin Sodium Injection, USP, 30,000 USP units per 30 mL (1,000 USP units per mL) multi-dose vial. The label states it is for intravenous or subcutaneous use, not for lock flush, and is derived from porcine intestinal mucosa. It includes storage instructions and manufacturer details for Medical Purchasing Solutions, LLC.*
FDA Label Image

7352.pdp (7352)

7352.pdp (7352)
Heparin Sodium Injection USP 1000 U per mL in a 30 mL multi-dose vial label. Indicates use for intravenous or subcutaneous injection, manufactured by Northstar Rx LLC and Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd. Distributed by Medical Purchasing Solutions, Scottsdale, AZ. Includes storage information, contents per mL, and standard disclaimers.*
FDA Label Image

Structure Of Heparin Sodium (Hep Structure)

Structure Of Heparin Sodium (Hep Structure)
Chemical structure diagram depicting the molecular components of Heparin Sodium, showing various sugar residues with functional groups including hydroxyl, sulfate, N-acetyl, and carboxyl groups, labeled with numbers 1 through 5.*

* 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.