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)

An instructional diagram of a prefilled single-dose syringe labeled 1 mL with increments at 0.5 mL. It highlights the syringe tip cap, which should be removed, the external collar which should not be removed, and the plunger rod. The syringe is labeled as made from porcine intestinal mucosa and manufactured for Meitheal Pharmaceuticals.*

FDA Label Image

Figure 2 (Hep0h 0005 02)

Instructional illustration showing how to use a vial or syringe. It depicts a hand twisting the cap or stopper off the vial or syringe, demonstrating the step required to access the medication inside.*

FDA Label Image

Figure (Hep0h 0005 03)

Chemical structure diagram showing multiple sugar units labeled (1) through (5), representing the structure of Heparin Sodium as a complex polysaccharide molecule.*

FDA Label Image

Logo (Hep0h 0005 04)

FDA Label Image

Barcode (Hep0h 0005 05)

A vial label for Heparin Sodium Injection, Solution with a concentration of 5000 USP units per mL. The label includes the proprietary and generic name Heparin Sodium. The labeler is Meitheal Pharmaceuticals Inc. The package is intended for intravenous or subcutaneous administration. The label also features a barcode and numeric code beneath it.*

FDA Label Image

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

Label for Heparin Sodium Injection, USP 5,000 USP units per mL in a 1 mL prefilled single-dose syringe. The label specifies intravenous or subcutaneous use and states the product is derived from porcine intestinal mucosa. It includes the NDC 71288-406-81 and the labeler Meitheal Pharmaceuticals Inc. The label highlights 'NOT for Lock Flush' and displays a barcode.*

FDA Label Image

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

Label for Heparin Sodium Injection, USP 5,000 USP units per mL in a 1 mL prefilled single-dose syringe. Intended for intravenous or subcutaneous use. The label includes manufacturer information for Meitheal Pharmaceuticals Inc., Chicago, IL, along with usage instructions and storage conditions. Product NDC 71288-406-81 is visible with a barcode and space for lot and expiration dates.*

FDA Label Image

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

Heparin Sodium Injection, USP 5,000 USP units per mL is shown as a prefilled single-dose syringe package label. The label indicates it is for intravenous or subcutaneous use and not for lock flush, with each pack containing 24 x 1 mL prefilled syringes. The labeler is Meitheal Pharmaceuticals Inc., and the package shows storage instructions along with a barcode and NDC 71288-406-82.*

* 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.