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  5. NDC Package Code: 57894-054-27 Stelara

NDC Package 57894-054-27 Stelara

Ustekinumab Solution Intravenous - 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:
57894-054-27
Package Description:
1 VIAL, SINGLE-USE in 1 BOX / 26 mL in 1 VIAL, SINGLE-USE
Product Code:
57894-054
Proprietary Name:
Stelara
Non-Proprietary Name:
Ustekinumab
Substance Name:
Ustekinumab
Usage Information:
Ustekinumab is used to treat plaque psoriasis, a certain type of arthritis (psoriatic arthritis), or certain bowel conditions (Crohn's disease, ulcerative colitis). It works by blocking certain natural proteins in your body (interleukin-12 and interleukin-23) that cause inflammation (swelling) in these conditions. Ustekinumab does not cure these diseases, but helps to lessen symptoms of the disease. It can help to decrease the amount of plaques in plaque psoriasis, decrease the number of swollen/painful joints in psoriatic arthritis, and decrease symptoms such as abdominal pain/cramping and diarrhea in Crohn's disease and ulcerative colitis.
11-Digit NDC Billing Format:
57894005427
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1654077 - ustekinumab 45 MG in 0.5 mL Injection
  • RxCUI: 1654077 - 0.5 ML ustekinumab 90 MG/ML Injection
  • RxCUI: 1654077 - ustekinumab 45 MG per 0.5 ML Injection
  • RxCUI: 1654079 - Stelara 45 MG in 0.5 mL Injection
  • RxCUI: 1654079 - 0.5 ML ustekinumab 90 MG/ML Injection [Stelara]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Janssen Biotech, Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • USTEKINUMAB 130 mg/26mL
    • Pharmacologic Class(es):
  • Interleukin-12 Antagonist - [EPC] (Established Pharmacologic Class)
  • Interleukin-12 Antagonists - [MoA] (Mechanism of Action)
  • Interleukin-23 Antagonist - [EPC] (Established Pharmacologic Class)
  • Interleukin-23 Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    BLA761044
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    09-23-2016
    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.

    * 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 57894-054-27 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    57894005427J3358Ustekinumab, iv inject, 1 mg1 MG261130130

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    57894-054-161 VIAL, SINGLE-USE in 1 BOX / 26 mL in 1 VIAL, SINGLE-USE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 57894-054-27?

    The NDC Packaged Code 57894-054-27 is assigned to a package of 1 vial, single-use in 1 box / 26 ml in 1 vial, single-use of Stelara, a human prescription drug labeled by Janssen Biotech, Inc.. The product's dosage form is solution and is administered via intravenous form.

    Is NDC 57894-054 included in the NDC Directory?

    Yes, Stelara with product code 57894-054 is active and included in the NDC Directory. The product was first marketed by Janssen Biotech, Inc. on September 23, 2016 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 NDC billing unit for package 57894-054-27?

    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 57894-054-27?

    The 11-digit format is 57894005427. 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
    5-3-257894-054-275-4-257894-0054-27