NDC Package 49281-620-10 Flublok Trivalent Northern Hemisphere

View Billable Units, 11-Digit Format, RxNorm

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:
49281-620-10
Package Description:
10 SYRINGE in 1 CARTON / .5 mL in 1 SYRINGE (49281-620-88)
Product Code:
Proprietary Name:
Flublok Trivalent Northern Hemisphere
Usage Information:
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. Flublok is approved for use in persons 18 years of age and older.
11-Digit NDC Billing Format:
49281062010
NDC to RxNorm Crosswalk:
  • 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]
Labeler Name:
Sanofi Pasteur Inc.
Sample Package:
No
FDA Application Number:
BLA125285
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
03-04-2024
End Marketing Date:
07-11-2024
Listing Expiration Date:
07-11-2024
Exclude Flag:
D
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 49281-620-10?

The NDC Packaged Code 49281-620-10 is assigned to a package of 10 syringe in 1 carton / .5 ml in 1 syringe (49281-620-88) of Flublok Trivalent Northern Hemisphere, labeled by Sanofi Pasteur Inc.. The product's dosage form is and is administered via form.

Is NDC 49281-620 included in the NDC Directory?

No, Flublok Trivalent Northern Hemisphere with product code 49281-620 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sanofi Pasteur Inc. on March 04, 2024 and its listing in the NDC Directory is set to expire on July 11, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 49281-620-10?

The 11-digit format is 49281062010. 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
5-3-249281-620-105-4-249281-0620-10