Licensed vaccine

Flulaval Quadrivalent

FDA-licensed vaccine · ID Biomedical Corporation of Quebec · STN BL 125163

Key facts

Trade name Flulaval Quadrivalent
Proper name Influenza Vaccine
Manufacturer ID Biomedical Corporation of Quebec
Submission tracking number (STN) BL 125163
FDA product areas Animal & Veterinary, Biologics, Vaccines
Recent FDA documents July 13, 2023 Approval Letter - FLULAVAL QUADRIVALENT, July 1, 2022 Approval Letter - FluLaval Quadrivalent, July 2, 2021 Approval Letter - FluLaval, July 2, 2020 Approval Letter - FluLaval, February 6, 2020 Approval Letter - FluLaval, July 2, 2019 Approval Letter - FluLaval, Package Insert - FLULAVAL QUADRIVALENT, June 29, 2018 Approval Letter - FluLaval Quadrivalent, July 7, 2017 Approval Letter - FluLaval Quadrivalent, Clinical Review - FluLaval and FluLaval Quadrivalent, Statistical Review Assay - FluLaval and FluLaval Quadrivalent, Statistical Review and Evaluation - FluLaval and FluLaval Quadrivalent
FDA page updated Jul 25, 2023
FDA product page fda.gov

At a glance

  • 1–9 FDA approval letters
  • 10–99 Supporting documents
  • 1–9 Product information documents
  • Yes Document full text searchable in Orca1

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA-licensed vaccines

The FDA's CBER licenses vaccines for use in the United States. Each product page links the approval letters, package inserts and supporting documents for that vaccine.

Source: U.S. Food and Drug Administration (FDA), Center for Biologics Evaluation and Research (CBER), Vaccines Licensed for Use in the United States · Source date:

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