Teva Draws on $1.75 Billion Bridge Financing in Connection with Pending Barr Acquisition
08 Dicembre 2008 - 7:15PM
Business Wire
Teva Pharmaceutical Industries Ltd. (NASDAQ: TEVA) today announced
that it has completed the drawdown of its combined $1.75�billion
bridge loan facilities with Bank Hapoalim B.M. and Bank Leumi USA.
The proceeds of the loans will be used towards funding Teva's
previously announced acquisition of Barr Pharmaceuticals, Inc.
(NYSE: BRL). Teva intends to fund the remaining cash portion of the
consideration by using its cash and marketable securities on hand.
"Teva has secured the necessary funds to complete the Barr
acquisition as well as to support the continued growth of our
business. We will continue to maintain a strong balance sheet
following the completion of the acquisition, with ample flexibility
for potential future strategic opportunities," said Eyal Desheh,
Teva's Chief Financial Officer. "We continue to make progress to
obtain the necessary regulatory approvals for this transaction,
which is expected to close by the end of this year." Teva
Pharmaceuticals USA, Inc. is the borrower under the facilities,
which mature in November 2009. Both facilities are guaranteed by
Teva. About Teva Teva Pharmaceutical Industries Ltd., headquartered
in Israel, is among the top 20 pharmaceutical companies in the
world and is the world's leading generic pharmaceutical company.
The Company develops, manufactures and markets generic and
innovative human pharmaceuticals and active pharmaceutical
ingredients, as well as animal health pharmaceutical products. Over
80 percent of Teva's sales are in North America and Europe. Safe
Harbor Statement under the U. S. Private Securities Litigation
Reform Act of 1995: This release contains forward-looking
statements, which express the current beliefs and expectations of
management. Such statements are based on management's current
beliefs and expectations and involve a number of known and unknown
risks and uncertainties that could cause our future results,
performance or achievements to differ significantly from the
results, performance or achievements expressed or implied by such
forward-looking statements. Important factors that could cause or
contribute to such differences include risks relating to: the
timing of the regulatory approvals and satisfaction of other
closing conditions for the pending Barr acquisition, our ability to
successfully develop and commercialize additional pharmaceutical
products, the introduction of competing generic equivalents, the
extent to which we may obtain U.S. market exclusivity for certain
of our new generic products and regulatory changes that may prevent
us from utilizing exclusivity periods, competition from brand-name
companies that are under increased pressure to counter generic
products, or competitors that seek to delay the introduction of
generic products, the impact of consolidation of our distributors
and customers, potential liability for sales of generic products
prior to a final resolution of outstanding patent litigation,
including that relating to the generic versions of Allegra� ,
Neurontin�, Lotrel� and Protonix�, the effects of competition on
our innovative products, especially Copaxone� sales, the impact of
pharmaceutical industry regulation and pending legislation that
could affect the pharmaceutical industry, the difficulty of
predicting U.S. Food and Drug Administration, European Medicines
Agency and other regulatory authority approvals, the regulatory
environment and changes in the health policies and structures of
various countries, our ability to achieve expected results though
our innovative R&D efforts, our ability to successfully
identify, consummate and integrate acquisitions, including the
pending acquisition of Barr Pharmaceuticals Inc., potential
exposure to product liability claims to the extent not covered by
insurance, dependence on the effectiveness of our patents and other
protections for innovative products, significant operations
worldwide that may be adversely affected by terrorism, political or
economical instability or major hostilities, supply interruptions
or delays that could result from the complex manufacturing of our
products and our global supply chain, environmental risks,
fluctuations in currency, exchange and interest rates, and other
factors that are discussed in this report and in our other filings
with the U.S. Securities and Exchange Commission ("SEC").
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