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  5. NDC Package Code: 66658-234-07 Kineret

NDC Package 66658-234-07 Kineret

Anakinra Injection, Solution Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
66658-234-07
Package Description:
7 SYRINGE, GLASS in 1 CARTON / .67 mL in 1 SYRINGE, GLASS
Product Code:
66658-234
Proprietary Name:
Kineret
Non-Proprietary Name:
Anakinra
Substance Name:
Anakinra
Usage Information:
This medication is used alone or with other medications to treat rheumatoid arthritis. It helps to slow joint damage and reduces the joint pain/swelling caused by rheumatoid arthritis so that you can move better. Anakinra is a man-made form of a natural protein (interleukin-1 receptor antagonist) made by the body. It helps to block the effects of another protein (interleukin-1) which can cause joint pain/swelling/stiffness. Anakinra is also used to treat a certain condition called Neonatal-Onset Multisystem Inflammatory Disease (NOMID). It helps to improve symptoms of the disease such as fever, rash, joint pain, vomiting, and headache.
11-Digit NDC Billing Format:
66658023407
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 727711 - anakinra 100 MG in 0.67 ML Prefilled Syringe
  • RxCUI: 727711 - 0.67 ML anakinra 149 MG/ML Prefilled Syringe
  • RxCUI: 727711 - anakinra 100 MG per 0.67 ML Prefilled Syringe
  • RxCUI: 727714 - Kineret 100 MG in 0.67 ML Prefilled Syringe
  • RxCUI: 727714 - 0.67 ML anakinra 149 MG/ML Prefilled Syringe [Kineret]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Swedish Orphan Biovitrum Ab (publ)
    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):
  • ANAKINRA 100 mg/.67mL
    • Pharmacologic Class(es):
  • Interleukin 1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Interleukin-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    BLA103950
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    12-15-2009
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    66658-234-284 CARTON in 1 CASE / 7 SYRINGE, GLASS in 1 CARTON (66658-234-07) / .67 mL in 1 SYRINGE, GLASS

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 66658-234-07?

    The NDC Packaged Code 66658-234-07 is assigned to a package of 7 syringe, glass in 1 carton / .67 ml in 1 syringe, glass of Kineret, a human prescription drug labeled by Swedish Orphan Biovitrum Ab (publ). The product's dosage form is injection, solution and is administered via subcutaneous form.

    Is NDC 66658-234 included in the NDC Directory?

    Yes, Kineret with product code 66658-234 is active and included in the NDC Directory. The product was first marketed by Swedish Orphan Biovitrum Ab (publ) on December 15, 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 66658-234-07?

    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 66658-234-07?

    The 11-digit format is 66658023407. 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
    5-3-266658-234-075-4-266658-0234-07