Heparin Sodium Injection, Solution
Product Images NDC 0409-2720

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 0409-2720). 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 of Heparin Sodium, showing the molecular components and their connectivity, including sulfate groups and sugar rings characteristic of this anticoagulant molecule.*

FDA Label Image

Hospira Logo (Heparin 02)

FDA Label Image

Principal Display Panel (1,000 USP Units/1 mL Vial Label)

Label for Heparin Sodium Injection USP 1,000 USP Units/mL in a 1 mL single-dose vial by Hospira, Inc. The label states that it is for intravenous or subcutaneous use, contains preservative, and is not for lock flush. The label includes an NDC and lot and expiration date placeholders.*

FDA Label Image

Principal Display Panel (1,000 USP Units/1 mL Vial Tray)

Packaging label for Heparin Sodium Injection, USP, 1000 USP Units/mL in 25 single-dose 1 mL vials. The label states it is for intravenous or subcutaneous use and contains preservative derived from porcine intestines. The labeler is Hospira, Inc. with NDC 0409-2720-01. Storage and contents information is also included.*

FDA Label Image

Principal Display Panel (10,000 USP Units/10 mL Vial Label)

Label for Heparin Sodium Injection, USP 10,000 USP Units/10 mL (1,000 USP Units/mL) multi-dose vial. The label indicates the product is for intravenous or subcutaneous use, derived from porcine intestines, with storage instructions and manufacturer Hospira, Inc. The label includes a warning 'NOT for LOCK FLUSH.'*

FDA Label Image

Principal Display Panel (10,000 USP Units/10 mL Vial Tray)

Heparin Sodium Injection, USP 10,000 USP Units/10 mL (1,000 USP Units/mL) multi-dose vial carton. The label states 'NOT for LOCK FLUSH,' indicates use for intravenous or subcutaneous administration, and notes the product is derived from porcine intestines. Labeler is Hospira, Inc. The package contains 25 vials of 10 mL each.*

FDA Label Image

Principal Display Panel (30,000 USP Units/30 mL Vial Label)

Label for Heparin Sodium Injection, USP, 1000 USP Units/mL in a 30 mL multi-dose vial. The label states 30,000 USP Units per 30 mL and indicates the solution is for intravenous or subcutaneous use. The product is distributed by Hospira, Inc., Lake Forest, IL. The label includes storage and dosage notes, along with lot and expiration date placeholders.*

FDA Label Image

Principal Display Panel (30,000 USP Units/30 mL Vial Tray)

Packaging label for Heparin Sodium Injection, USP, 30,000 USP Units/30 mL (1,000 USP Units/mL) by Hospira, Inc. The label indicates a carton containing 25 multi-dose vials of 30 mL each. It is for intravenous or subcutaneous use and sourced from porcine intestines. The label includes warning 'NOT for LOCK FLUSH' and displays the NDC 0409-2720-03.*

FDA Label Image

Principal Display Panel (10,000 USP Units/1 mL Vial Label)

Heparin Sodium Injection USP label for a 1 mL single-dose vial with a strength of 10,000 USP Units/mL. The label indicates it is for intravenous or subcutaneous use and includes warnings 'NOT for LOCK FLUSH' in red at the top and bottom. Distributed by Hospira, Inc., Lake Forest, IL. The label also shows space for lot number and expiration date information.*

FDA Label Image

Principal Display Panel (10,000 USP Units/1 mL Vial Tray)

Carton label for Heparin Sodium Injection USP, 10,000 USP Units/mL, in 25 x 1 mL single-dose vials. The label indicates the product is for intravenous or subcutaneous use, sourced from porcine intestines, contains preservative, and is not for lock flush. Labeler is Hospira, Inc.*

FDA Label Image

Principal Display Panel (5,000 USP Units/1 mL Vial Label)

Label for Heparin Sodium Injection, USP 5,000 USP Units/mL in a 1 mL single-dose vial. The label states it is for intravenous or subcutaneous use, from porcine intestines, contains preservative, and is distributed by Hospira, Inc. Prominent warnings indicate it is not for lock flush.*

FDA Label Image

Principal Display Panel (5,000 USP Units/1 mL Vial Tray)

Packaging label for Heparin Sodium Injection, USP 5,000 USP Units/mL in 25 single-dose 1 mL vials. The label indicates use for intravenous or subcutaneous administration, contains preservative, and is derived from porcine intestines. Labeler is Hospira, Inc. The packaging states 'NOT for LOCK FLUSH' and includes NDC numbers 0409-2723-01 and 0409-2723-30.*

FDA Label Image

Principal Display Panel (50,000 USP Units/10 mL Vial Label)

Heparin Sodium Injection, USP 50,000 USP Units/10 mL (5,000 USP Units/mL) multi-dose vial label. It is for intravenous or subcutaneous use, derived from porcine intestines. The label includes storage instructions and notes it is Rx only, distributed by Hospira, Inc., Lake Forest, IL.*

FDA Label Image

Principal Display Panel (50,000 USP Units/10 mL Vial Tray)

Heparin Sodium Injection, USP 50,000 USP Units/10 mL (5,000 USP Units/mL) multi-dose vial carton from Hospira, Inc. The label states it is for intravenous or subcutaneous use and derived from porcine intestines. The package contains 25 vials of 10 mL each and includes storage and handling information.*

* 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.