1. Labeler Index
  2. Fresenius Kabi Usa, Llc
  3. 63323-262
  4. NDC Package Code: 63323-262-55 Heparin Sodium

NDC Package 63323-262-55 Heparin Sodium

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

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. Frequently Asked Questions

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:
63323-262-55
Package Description:
25 VIAL in 1 TRAY / 1 mL in 1 VIAL
Product Code:
63323-262
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:
63323026255
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1361226 - heparin sodium, porcine 1000 UNT/ML Injectable Solution
  • RxCUI: 1361574 - heparin sodium, porcine 20,000 UNT/ML Injectable Solution
  • RxCUI: 1361574 - heparin sodium, porcine 20000 UNT/ML Injectable Solution
  • RxCUI: 1361615 - heparin sodium, porcine 5000 UNT/ML Injectable Solution
  • RxCUI: 1362831 - heparin sodium, porcine 10,000 UNT/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Fresenius Kabi Usa, Llc
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • HEPARIN SODIUM 5000 [USP'U]/mL
  • HEPARIN SODIUM 5000 [USP'U]/mL
  • HEPARIN SODIUM 5000 [USP'U]/mL
  • HEPARIN SODIUM 5000 [USP'U]/mL
    • Pharmacologic Class(es):
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Heparin - [CS]
  • Unfractionated Heparin - [EPC] (Established Pharmacologic Class)
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Heparin - [CS]
  • Unfractionated Heparin - [EPC] (Established Pharmacologic Class)
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Heparin - [CS]
  • Unfractionated Heparin - [EPC] (Established Pharmacologic Class)
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Heparin - [CS]
  • Unfractionated Heparin - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA017029
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-25-2020
    Listing Expiration Date:
    12-31-2024
    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.

    * Please review the disclaimer below.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 63323-262-55 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    63323026255J1644Inj heparin sodium per 1000u1000 UNITS1255125

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    63323-262-0125 VIAL in 1 TRAY / 1 mL in 1 VIAL
    63323-262-0625 VIAL in 1 TRAY / 1 mL in 1 VIAL (63323-262-03)
    63323-262-2625 VIAL in 1 TRAY / 1 mL in 1 VIAL (63323-262-09)
    63323-262-3625 VIAL in 1 TRAY / 1 mL in 1 VIAL (63323-262-11)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63323-262-55?

    The NDC Packaged Code 63323-262-55 is assigned to a package of 25 vial in 1 tray / 1 ml in 1 vial of Heparin Sodium, a human prescription drug labeled by Fresenius Kabi Usa, Llc. The product's dosage form is injection, solution and is administered via intravenous; subcutaneous form.

    Is NDC 63323-262 included in the NDC Directory?

    Yes, Heparin Sodium with product code 63323-262 is active and included in the NDC Directory. The product was first marketed by Fresenius Kabi Usa, Llc on March 25, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 63323-262-55?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 63323-262-55?

    The 11-digit format is 63323026255. 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
    5-3-263323-262-555-4-263323-0262-55