1. Home
  2. Labeler Index
  3. Organon Llc
  4. 78206-202
  5. NDC Package Code: 78206-202-01 Tofidence

NDC Package 78206-202-01 Tofidence

Tocilizumab Injection Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
78206-202-01
Package Description:
1 VIAL, SINGLE-DOSE in 1 CARTON / 20 mL in 1 VIAL, SINGLE-DOSE
Product Code:
78206-202
Proprietary Name:
Tofidence
Non-Proprietary Name:
Tocilizumab
Substance Name:
Tocilizumab
Usage Information:
This medication is used alone or with other medications to treat moderate to severe rheumatoid arthritis in adults. It is also used to treat rheumatoid arthritis in children (such as systemic juvenile idiopathic arthritis-SJIA, polyarticular juvenile idiopathic arthritis-PJIA). It helps to reduce pain and swelling due to rheumatoid arthritis. Tocilizumab may also be used to treat a reaction (Cytokine Release Syndrome-CRS) caused by certain cancer treatments. Tocilizumab belongs to a class of drugs known as Interleukin-6 (IL-6) blockers. It works by blocking IL-6, a substance made by the body that causes swelling (inflammation).
11-Digit NDC Billing Format:
78206020201
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Organon Llc
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
TOCILIZUMAB 400 mg/20mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
BLA761354
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
07-03-2025
Listing Expiration Date:
12-31-2026
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 78206-202-01?

The NDC Packaged Code 78206-202-01 is assigned to a package of 1 vial, single-dose in 1 carton / 20 ml in 1 vial, single-dose of Tofidence, a human prescription drug labeled by Organon Llc. The product's dosage form is injection and is administered via intravenous form.

Is NDC 78206-202 included in the NDC Directory?

Yes, Tofidence with product code 78206-202 is active and included in the NDC Directory. The product was first marketed by Organon Llc on July 03, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 78206-202-01?

The 11-digit format is 78206020201. 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
5-3-278206-202-015-4-278206-0202-01