NDC Package 57894-060-03 Stelara

Ustekinumab Injection, Solution 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:
57894-060-03
Package Description:
1 SYRINGE in 1 CARTON / .5 mL in 1 SYRINGE
Product Code:
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:
57894006003
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:
    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):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    BLA125261
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    09-25-2009
    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 57894-060-03 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    57894006003J3357Ustekinumab sub cu inj, 1 mg1 MG0.514545

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    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    57894-060-021 VIAL, SINGLE-USE in 1 CARTON / .5 mL in 1 VIAL, SINGLE-USE
    57894-060-041 SYRINGE in 1 CARTON / .5 mL in 1 SYRINGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 57894-060-03?

    The NDC Packaged Code 57894-060-03 is assigned to a package of 1 syringe in 1 carton / .5 ml in 1 syringe of Stelara, a human prescription drug labeled by Janssen Biotech, Inc.. The product's dosage form is injection, solution and is administered via subcutaneous form.

    Is NDC 57894-060 included in the NDC Directory?

    Yes, Stelara with product code 57894-060 is active and included in the NDC Directory. The product was first marketed by Janssen Biotech, Inc. on September 25, 2009 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 57894-060-03?

    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 57894-060-03?

    The 11-digit format is 57894006003. 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
    5-3-257894-060-035-4-257894-0060-03