NDC Package 72603-336-25 Heparin Sodium

Injection Intravenous; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
72603-336-25
Package Description:
25 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE (72603-336-01)
Product Code:
Proprietary Name:
Heparin Sodium
Non-Proprietary Name:
Heparin Sodium
Substance Name:
Heparin Sodium
Usage Information:
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.
11-Digit NDC Billing Format:
72603033625
NDC to RxNorm Crosswalk:
  • RxCUI: 1658647 - heparin sodium, porcine 2000 UNT in 2 ML Injection
  • RxCUI: 1658647 - 2 ML heparin sodium, porcine 1000 UNT/ML Injection
  • RxCUI: 1658647 - heparin sodium, porcine 2000 UNT per 2 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Northstar Rxllc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA211005
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-01-2024
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    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.

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    Frequently Asked Questions

    What is NDC 72603-336-25?

    The NDC Packaged Code 72603-336-25 is assigned to a package of 25 vial, single-dose in 1 carton / 2 ml in 1 vial, single-dose (72603-336-01) of Heparin Sodium, a human prescription drug labeled by Northstar Rxllc. The product's dosage form is injection and is administered via intravenous; subcutaneous form.

    Is NDC 72603-336 included in the NDC Directory?

    Yes, Heparin Sodium with product code 72603-336 is active and included in the NDC Directory. The product was first marketed by Northstar Rxllc on April 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 72603-336-25?

    The 11-digit format is 72603033625. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-272603-336-255-4-272603-0336-25