Heparin Sodium Injection, Solution
Product Images NDC 71288-406

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 71288-406). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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.

FDA Label Image

Figure 1 (Hep0h 0005 01)

FDA Label Image

Figure 2 (Hep0h 0005 02)

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Figure (Hep0h 0005 03)

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Logo (Hep0h 0005 04)

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Barcode (Hep0h 0005 05)

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Syringe Label (Hep0h 0005 06)

This is a description for a medication product that is intended to be used either intravenously or subcutaneously. The medication is extracted from porcine intestinal mucosa and is sold in a 1mL pre-filled single-dose syringe. The medication is manufactured specifically for Meitheal Pharmaceuticals and the NDC number is 71288-406-81. The medication has 5,000 USP units per mL and should not be used for lock flush purposes.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Blister Pack Label (Hep0h 0005 07)

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Carton (Hep0h 0005 08)

This is a description of a medication called "Sodium Injection, USP 5,000" which is made from porcine intestinal mucosa. It is used for intravenous or subcutaneous use and each mL contains heparin sodium, sodium chloride, and benzyl alcohol. It is not for lock flush and its usual dosage is detailed in the package insert. The medication needs to be stored at a specific temperature and the syringe used for dispensing should not be placed on a sterile field. The medication comes in a pre-filled single-dose syringe with a container closure that is not made with natural rubber latex.*

* 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.