Heparin Sodium Injection
Product Images NDC 72603-224

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 72603-224). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

Principal Display Panel – Heparin Sodium Injection, Usp 20,000 Usp Units Carton (Hep Carton V1)

Packaging label for Heparin Sodium Injection USP 20,000 units per mL by NorthStar RxLLC. The label states that the drug is for intravenous or subcutaneous use, supplied in multi-dose vials of 25 x 1 mL. It includes storage instructions, manufacturer details, and a barcode. The label prominently features a red circular warning stating 'NOT for Lock Flush.'*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 20,000 Usp Units Vial Label (Hep Container V1)

Label for Heparin Sodium Injection, USP 20,000 USP units per mL, in a 1 mL multi-dose vial. The label notes it is not for lock flush and indicates intravenous or subcutaneous use. Manufactured in China for NorthStar Rx LLC, with porcine intestinal mucosa as the source. Includes lot and expiration date fields.*

FDA Label Image

Structural Formula (Hep Structure V1)

Chemical structure diagram illustrating five components labeled (1) through (5), depicting molecular structures consistent with heparin sodium's chemical composition. The diagram shows various sugar ring structures with sulfate and acetyl functional groups attached, characteristic of heparin sodium.*

* 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.