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Fluarix Quadrivalent FDA Approval History

Last updated by Judith Stewart, BPharm on Oct 28, 2020.

FDA Approved: Yes (First approved December 14, 2012)
Brand name: Fluarix Quadrivalent
Generic name: influenza virus vaccine, inactivated
Dosage form: Injection
Company: GlaxoSmithKline
Treatment for: Influenza Prophylaxis

Fluarix Quadrivalent is an inactivated influenza virus vaccine indicated for the prevention of influenza disease in people aged 6 months and older.

Development timeline for Fluarix Quadrivalent

DateArticle
Jan 11, 2018Approval GSK Receives FDA Approval for Expanded Indication for Fluarix Quadrivalent (Influenza Vaccine) for Persons 6 Months and Older
Dec 17, 2012Approval FDA Approves GlaxoSmithKline's Fluarix Quadrivalent - Four-strain Seasonal Influenza Vaccine for Use in the U.S.
Oct 19, 2009Approval FDA Approves Seasonal Influenza Vaccine Fluarix for Pediatric Use
Aug 31, 2005Approval Fluarix GlaxoSmithKline - Treatment for Influenza Vaccination
May 25, 2005GlaxoSmithKline Submits Biologics License Application for FDA Approval of Fluarix

See also

Fluarix Quadrivalent (influenza virus vaccine, inactivated) Consumer information

Further information

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