Flublok Trivalent Northern Hemisphere Injection
NDC Package 49281-725-10
Package Information
Flublok Trivalent Northern Hemisphere (influenza a virus a/west virginia/30/2022 (h1n1) recombinant hemagglutinin antigen, influenza a virus a/district of columbia/27/2023 (h3n2) recombinant hemagglutinin antigen, and influenza b virus b/austria/1359417/2021 recombinant hemagglutinin antigen) injection is flublok is a vaccine indicated for active immunization for the prevention of disease caused by influenza A virus subtypes and influenza type B virus contained in the vaccine. This formulation utilizes a injection delivery system. Marketed by Sanofi Pasteur Inc., this product is identified by NDC 49281-725 and is authorized under FDA application BLA125285.
Identification & Billing
- RxCUI: 2719304 - influenza virus vaccine 2025-2026 (trivalent - District of Columbia/West Virginia/Austria) 0.5 ML Prefilled Syringe
- RxCUI: 2719304 - 0.5 ML influenza A virus A/District of Columbia/27/2023 (H3N2) antigen 0.09 MG/ML / influenza A virus A/West Virginia/30/2022 (H1N1) antigen 0.09 MG/ML / influenza B virus B/Austria/1359417/2021 antigen 0.09 MG/ML Prefilled Syringe
- RxCUI: 2719311 - Flublok 2025-2026 vaccine 0.5 ML Prefilled Syringe
- RxCUI: 2719311 - 0.5 ML influenza A virus A/District of Columbia/27/2023 (H3N2) antigen 0.09 MG/ML / influenza A virus A/West Virginia/30/2022 (H1N1) antigen 0.09 MG/ML / influenza B virus B/Austria/1359417/2021 antigen 0.09 MG/ML Prefilled Syringe [Flublok 2025-2026]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 49281 - Sanofi Pasteur Inc.
- 49281-725 - Flublok Trivalent Northern Hemisphere
- 49281-725-10 - 10 SYRINGE in 1 CARTON / .5 mL in 1 SYRINGE (49281-725-88)
- 49281-725 - Flublok Trivalent Northern Hemisphere
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.
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.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 49281-725-10 identifies a specific commercial package of 10 syringe in 1 carton / .5 ml in 1 syringe (49281-725-88) of Flublok Trivalent Northern Hemisphere, a vaccine label labeled by Sanofi Pasteur Inc.. This injection is formulated for intramuscular use and contains influenza a virus a/district of columbia/27/2023 (h3n2) recombinant hemagglutinin antigen; influenza a virus a/west virginia/30/2022 (h1n1) recombinant hemagglutinin antigen; influenza b virus b/austria/1359417/2021 recombinant hemagglutinin antigen 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 Sanofi Pasteur Inc. on July 01, 2025.
How is this Sanofi Pasteur Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 49281072510. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.