Heparin Sodium Injection, Solution
Product Images NDC 0409-1005

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 0409-1005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Chemical Structure (Heparin 01)

Chemical structure diagram depicting the molecular components of Heparin Sodium, showing its polysaccharide chains and functional groups as part of the active ingredient’s chemical composition.*

FDA Label Image

Chemical Structure (Heparin 02)

Chemical structure of heparin sodium monohydrate, showing a molecular formula including carboxyl and hydroxyl groups with one molecule of water (H2O).*

FDA Label Image

Logo (Heparin 03)

FDA Label Image

Principal Display Panel (500 mL Bag)

Label for Heparin Sodium 1,000 USP Units per 500 mL in 0.9% Sodium Chloride Injection by Hospira, Inc. The bag contains a 500 mL solution with 2 USP Units/mL concentration. The label includes dosage form details, single-dose container use, and a note that the product contains DEHP.*

FDA Label Image

Principal Display Panel (1,000 mL Bag)

Label for Heparin Sodium 2000 USP Units per 1000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, distributed by Hospira, Inc. The label includes dosage information, warnings, and usage instructions. The container is a single-dose intravenous solution and marked with the NDC code 0409-7620-49.*

FDA Label Image

Principal Display Panel (Bag Overwrap)

A text panel with instructions on how to open the product overwrap by tearing at the notch and checking for leaks. It includes storage recommendations to keep at room temperature (25°C), protect from excessive heat and freezing, and a note stating the product is not made with natural rubber latex. The panel also displays recycling information for HDPE plastic and three "NO COPY NO INK" marks in blue boxes on the borders.*

FDA Label Image

Principal Display Panel (500 mL Bag Label)

Label for Heparin Sodium injection, 1,000 USP Units/500 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection. The 500 mL bag contains Heparin Sodium at 200 USP Units per 100 mL with buffers and no natural rubber latex. Distributed by Hospira, Inc. The NDC is 0409-1005-01, and the label includes usage and storage instructions, a barcode, lot and expiration placeholders, and recycling information.*

FDA Label Image

Principal Display Panel (1000 mL Bag Label)

Heparin Sodium 2,000 USP Units per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection label from Hospira, Inc. The label specifies each 100 mL contains 200 USP Units of Heparin Sodium with additional ingredients and usage instructions. It is packaged in a single-dose container for intravenous use with storage and disposal guidelines, and includes a barcode and lot/expiration placeholders.*

* 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.