Heparin Sodium Injection, Solution
NDC Package 0409-2721-01
Package Information
Heparin Sodium injection is a medication used to prevent and treat blood clots. This formulation utilizes a injection, solution delivery system. Marketed by Hospira, Inc., this product is identified by NDC 0409-2721 and is authorized under FDA application ANDA090571.
Identification & Billing
- RxCUI: 1361226 - heparin sodium, porcine 1000 UNT/ML Injectable Solution
- RxCUI: 1361615 - heparin sodium, porcine 5000 UNT/ML Injectable Solution
- RxCUI: 1658637 - heparin sodium, porcine 10,000 UNT in 1 ML Injection
- RxCUI: 1658637 - 1 ML heparin sodium, porcine 10000 UNT/ML Injection
- RxCUI: 1658637 - heparin sodium, porcine 10,000 UNT per 1 ML Injection
Clinical Specifications
- Intravenous - Administration within or into a vein or veins.
- Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Regulatory & Marketing
Hierarchy Structure
- 0409 - Hospira, Inc.
- 0409-2721 - Heparin Sodium
- 0409-2721-01 - 25 VIAL, SINGLE-DOSE in 1 TRAY / 1 mL in 1 VIAL, SINGLE-DOSE (0409-2721-30)
- 0409-2721 - Heparin Sodium
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0409-2721-01 identifies a specific commercial package of 25 vial, single-dose in 1 tray / 1 ml in 1 vial, single-dose (0409-2721-30) of Heparin Sodium, a human prescription drug labeled by Hospira, Inc.. This injection, solution is formulated for intravenous; subcutaneous use and contains heparin sodium as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hospira, Inc. on August 31, 2009. The current certification is valid through December 31, 2027.
What are the primary indications for this medication?
This medication is used to prevent and treat blood clots. It may be used to prevent and treat blood clots in the lungs/legs (including in patients with atrial fibrillation). It may be used to treat certain blood clotting disorders. It may also be used to prevent blood clots after surgery, during dialysis, during blood transfusions, when collecting blood samples, or when a person is unable to move for a long time. Heparin helps to keep blood flowing smoothly by making a certain natural substance in your body (anti-clotting protein) work better. It is known as an anticoagulant.
How is this Hospira, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00409272101. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.