On Dec. 12, 2014, Sanofi Pasteur announced the U.S. Food and Drug Administration (FDA) had approved the supplemental biologics license application (sBLA) for Fluzone Intradermal Quadrivalent vaccine.

Fluzone Intradermal vaccine, which has been available in trivalent formulation for three years, became available in a quadrivalent formulation to help protect against four strains of influenza virus.

Fluzone Intradermal Quadrivalent vaccine is indicated for adults 18 through 64 years of age for active immunization for the prevention of influenza caused by influenza A subtype viruses and type B viruses contained in the vaccine.