NDC Package 57894-420-01 Sylvant

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:

57894-420-01

Package Description:

1 VIAL, SINGLE-USE in 1 CARTON / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE

Product Code:

57894-420

Proprietary Name:

Sylvant

Usage Information:

Siltuximab is used to treat a certain rare illness (multicentric Castleman's disease - MCD) if you do not have HIV or herpes infections. Siltuximab blocks a certain natural substance that affects the immune system. Siltuximab can improve the symptoms of MCD including lumps under the skin, fever, weakness or tiredness, or night sweats.

11-Digit NDC Billing Format:

57894042001

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

1 EA

Labeler Name:

Janssen Biotech, Inc.

Sample Package:

FDA Application Number:

BLA125496

Marketing Category:

BLA - A product marketed under an approved Biologic License Application.

Start Marketing Date:

04-23-2014

End Marketing Date:

01-31-2021

Listing Expiration Date:

01-31-2021

Exclude Flag:

Code Structure:

57894 - Janssen Biotech, Inc.
- 57894-420 - Sylvant
  - 57894-420-01 - 1 VIAL, SINGLE-USE in 1 CARTON / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE

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 57894-420-01?

The NDC Packaged Code 57894-420-01 is assigned to a package of 1 vial, single-use in 1 carton / 1 injection, powder, lyophilized, for solution in 1 vial, single-use of Sylvant, labeled by Janssen Biotech, Inc.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 57894-420 included in the NDC Directory?

No, Sylvant with product code 57894-420 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Janssen Biotech, Inc. on April 23, 2014 and its listing in the NDC Directory is set to expire on January 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 57894-420-01?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

What is the 11-digit format for NDC 57894-420-01?

The 11-digit format is 57894042001. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	57894-420-01	5-4-2	57894-0420-01

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