Pharmaceutical Manufacturer to
Pay
Ohio $3.8 Million
(COLUMBUS,
Ohio) -- Ohio Attorney
General Mike DeWine announced today that Ohio has joined with other
states and
the federal government in a $500 million dollar settlement to resolve
civil and
criminal allegations against a pharmaceutical manufacturer in India.
Investigators
said Ranbaxy, a
generic pharmaceutical manufacturer based in Gurgaon, India, introduced
adulterated drugs into interstate commerce.
As a result, false or fraudulent claims
were submitted to Ohio's Medicaid
Program.
The
total portion of the settlement
amount recovered by Ohio is $3.8 million.
"The
knowing manufacture and
distribution of adulterated drugs with the intent to defraud or mislead
presents a serious risk to public safety, and it is also a very costly
crime," said Attorney General DeWine.
"Medicaid reimbursed for millions of
dollars of medications that
were potentially ineffective or unsafe."
The
investigation resulted from
whistleblower action filed in the United States District Court for the
District
of Maryland under the federal False Claims Act.
The whistleblower's complaint alleged
that Ranbaxy knowingly
manufactured, distributed and sold generic pharmaceutical products –
whose
strength, purity and/or quality fell below the standards required by
the
FDA. The products
at issue consisted of
26 generic pharmaceutical products manufactured at its facilities in
Paonta
Sahib and Dewas, India, at various times between April 1, 2003 and
September
16, 2010.
Ranbaxy
has agreed to pay the
states and the federal government $350 million dollars in civil damages
and
penalties to resolve civil allegations of poor manufacturing practices
in two
Indian manufacturing plants.
$266,729,715.10 of this amount will go
to the Medicaid programs, which
is funded jointly by the states and the federal government.
The
remaining $83,270,284.86 is
designated for other federal health care programs affected by Ranbaxy's
conduct.
Additionally,
Ranbaxy USA, a
subsidiary, has pled guilty to seven felony counts alleging violations
of the
U.S. Food, Drug, and Cosmetic Act, and has agreed to pay $150 million
dollars
in criminal fines and forfeitures.
Ranbaxy
entered into a consent
decree in January 2012 with the federal government to address
outstanding
current good manufacturing practice (cGMP) and data integrity issues in
the two
Indian manufacturing plants at issue.
These provisions include a wide range of
actions to correct its
violations and to ensure that the violations do not occur again.
A
team from the National
Association of Medicaid Fraud Control Units (NAMFCU) conducted the
settlement
negotiations with Ranbaxy on behalf of the states.
|