May 24, 2019
Philip Morris International Announces U.S. Food and Drug Administration Authorization For Sale of IQOS in the United States
Unlike cigarettes, the IQOS system heats — but does not burn
— tobacco. It is the first electrically heated tobacco product to
qualify for sale in the U.S. pursuant to the 2009 law that empowers
Commenting on the FDA’s announcement, André Calantzopoulos, PMI’s Chief Executive Officer, said:
“The FDA’s decision to authorize IQOS in the U.S. is an
important step forward for the approximately 40 million American men and
women who smoke. Some will quit. Most won’t, and for them IQOS offers
a smoke-free alternative to continued smoking. In just two
years, 7.3 million people around the world have abandoned cigarettes and
switched completely to IQOS. Today’s decision by
He added, “The order sets out clear commercialization guidelines,
including marketing requirements, that maximize the opportunity for
adults to switch from cigarettes, while minimizing unintended use. We
fully support this objective.
PMI will bring IQOS to the U.S. market through an exclusive
license with
PMI submitted a comprehensive body of scientific evidence in support of
the PMTAs and of the parallel applications for IQOS as a
“Modified Risk Tobacco Product”, which
Note to Editor
View source version on businesswire.com: https://www.businesswire.com/news/home/20190430006048/en/
Source:
Corey Henry
Philip Morris International Media Office
T. +1
(202) 679 7296
E. corey.henry@pmi.com
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