Vyvgart Hytrulo Injection, Solution
NDC Package 73475-1221-4

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Vyvgart Hytrulo (efgartigimod alfa and hyaluronidase (human recombinant)) injection is vYVGART HYTRULO is indicated for the treatment of generalized myasthenia gravis (gMG) in adult patients who are anti-acetylcholine receptor (AChR) antibody positive. This formulation utilizes a injection, solution delivery system. Marketed by Argenx Us, this product is identified by NDC 73475-1221 and is authorized under FDA application BLA761304.

Identification & Billing

NDC Package Code
73475-1221-4
Package Description
4 SYRINGE, GLASS in 1 CARTON / 5 mL in 1 SYRINGE, GLASS
Product Code
11-Digit Billing Format
73475122104
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 2639951 - efgartigimod alfa-hyaluronidase-qvfc 1008 MG / 11,200 UNT in 5.6 ML Injection
  • RxCUI: 2639951 - 5.6 ML efgartigimod alfa-qvfc 180 MG/ML / hyaluronidase-qvfc 2000 UNT/ML Injection
  • RxCUI: 2639951 - efgartigimod alfa-hyaluronidase-qvfc 1008 MG / 11,200 UNT per 5.6 ML Injection
  • RxCUI: 2639951 - efgartigimod alfa-qvfc 1008 MG / hyaluronidase-qvfc 11,200 UNT per 5.6 ML Injection
  • RxCUI: 2639957 - VYVGART Hytrulo 1008 MG / 11,200 UNT in 5.6 ML Injection

Clinical Specifications

Proprietary Name
Vyvgart Hytrulo
Non-Proprietary Name
Efgartigimod Alfa And Hyaluronidase (human Recombinant)
Substance Name
Efgartigimod Alfa; Hyaluronidase (human Recombinant)
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
Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Usage Information
VYVGART HYTRULO is indicated for the treatment of generalized myasthenia gravis (gMG) in adult patients who are anti-acetylcholine receptor (AChR) antibody positive.

Regulatory & Marketing

Labeler Name
Argenx Us
Product Type
Human Prescription Drug
FDA Application #
BLA761304
Marketing Category
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date
04-10-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Billing & HCPCS Mapping

To facilitate insurance claims and reimbursement, this drug package is mapped to specific HCPCS administrative codes. This crosswalk aligns clinical data with the billing standards used in ASP (Average Sales Price), AWP, and OPPS payment systems. Use the cards below to identify the correct billable units for provider claims.

Source: ASP
Inj efgart-alfa 2mg hya-qvfc
HCPCS Dosage 2 MG
Units / Pkg 2000

Note for Medical Coders: These mappings are synthesized from various CMS datasets including OPPS, PrEP, and DAC (Data Analysis and Coding) contractors. Always confirm unit conversions against the current quarter's pricing files before final submission.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (73475-1221). Click a package code to view its specific billing and regulatory data.

1 SYRINGE, GLASS in 1 CARTON / 5 mL in 1 SYRINGE, GLASS

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 73475-1221-4 identifies a specific commercial package of 4 syringe, glass in 1 carton / 5 ml in 1 syringe, glass of Vyvgart Hytrulo, a human prescription drug labeled by Argenx Us. This injection, solution is formulated for subcutaneous use and contains efgartigimod alfa; hyaluronidase (human recombinant) as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Argenx Us on April 10, 2025. The current certification is valid through December 31, 2027.

How is this Argenx Us product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73475122104. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
73475-1221-4
11-Digit CMS (5-4-2)
73475-1221-04

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.