NDC Package 55154-1423-8 Xarelto

Rivaroxaban Tablet, Film Coated Oral - 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:
55154-1423-8
Package Description:
4440 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Xarelto
Non-Proprietary Name:
Rivaroxaban
Substance Name:
Rivaroxaban
Usage Information:
Rivaroxaban is used to prevent blood clots from forming due to a certain irregular heartbeat (atrial fibrillation) or after hip or knee replacement surgery. It is also used to prevent blood clots from forming in high-risk patients with limited mobility during their hospital stay and after discharge. In addition, rivaroxaban is used to treat blood clots (such as in deep vein thrombosis-DVT or pulmonary embolus-PE) and to prevent the blood clots from forming again. Rivaroxaban is an anticoagulant that works by blocking certain clotting proteins in your blood.
11-Digit NDC Billing Format:
55154142308
NDC to RxNorm Crosswalk:
  • RxCUI: 1114198 - rivaroxaban 10 MG Oral Tablet
  • RxCUI: 1114202 - Xarelto 10 MG Oral Tablet
  • RxCUI: 1114202 - rivaroxaban 10 MG Oral Tablet [Xarelto]
  • RxCUI: 1232082 - rivaroxaban 15 MG Oral Tablet
  • RxCUI: 1232084 - Xarelto 15 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cardinal Health 107, Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA202439
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-05-2011
    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.

    Frequently Asked Questions

    What is NDC 55154-1423-8?

    The NDC Packaged Code 55154-1423-8 is assigned to a package of 4440 tablet, film coated in 1 bottle, plastic of Xarelto, a human prescription drug labeled by Cardinal Health 107, Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 55154-1423 included in the NDC Directory?

    Yes, Xarelto with product code 55154-1423 is active and included in the NDC Directory. The product was first marketed by Cardinal Health 107, Llc on November 05, 2011 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 11-digit format for NDC 55154-1423-8?

    The 11-digit format is 55154142308. 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 5-4-1 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
    5-4-155154-1423-85-4-255154-1423-08