Synovics Pharmaceuticals Announces Execution of Hormonal Manufacture and Supply Contract
24 Juni 2008 - 4:30PM
PR Newswire (US)
FORT LAUDERDALE, Fla., June 24 /PRNewswire-FirstCall/ -- Synovics
Pharmaceuticals, Inc. (OTC:SYVC) (BULLETIN BOARD: SYVC) , a
specialty pharmaceutical company, today announced that its wholly
owned subsidiary, ANDAPharm, LLC (ANDAPharm) signed a contract with
a leading pharmaceutical company for the manufacturing and supply
of a hormonal prescription drug. The potential annual sales by
ANDAPharm with this product, including an earlier contract with a
second pharmaceutical company, are between $7.5 million and $8
million. "ANDAPharm's sales are an outgrowth of our investment in a
specialized containment suite at our facility in Ft. Lauderdale for
manufacturing and packaging of hormonal and other products
requiring specialized facilities and handling," stated John S.
Copanos, ANDAPharm's founder and VP of Business Development for
Synovics. "We are very pleased with the success of this product and
are looking forward to the possibility of further supply contracts
for drugs produced in this containment suite. We have several
hormonal prescription drugs under various stages of development and
view this specialized category as a unique opportunity for our
Company. Specifically, we expect to launch our second generic
prescription hormonal, subject to anticipated authorization by the
FDA, between the third and fourth quarters of this year, and we
have our third hormonal drug in bio-studies for submission to the
FDA. We are acquiring two additional hormonal drugs via technology
transfers and intend to continue to develop and grow our pipeline
of these products as we leverage our containment suite capacity and
build this business with our productive and experienced staff."
"The Company's specialized containment suite allows us to focus on
the development and commercialization of products that have a
higher barrier to entry and, therefore, potentially less
competition," commented Ronald Howard Lane, Ph.D., Synovics'
Chairman and Chief Executive Officer. "Our plans call for the
Company to continue to develop niche drug products, both
prescription and over-the-counter (OTC), in categories where we
have specialized manufacturing or licensing advantages (such as
Drug Enforcement Administration, "DEA," licenses). Combined with
our advantaged active pharmaceutical ingredient ("API") sourcing,
and the new product development and manufacturing capacity we are
acquiring through our growing strategic Front-End relationships in
India, we believe we have we have unique and profitable
opportunities to continue to grow our business." About Synovics:
Synovics is a specialty pharmaceutical company engaged in the
development, manufacturing and commercialization of prescription
and OTC drugs. The Company has two operating subsidiaries, Kirk
Pharmaceuticals, LLC and ANDAPharm, LLC, which manufactures and
sells OTC and prescriptions private label or "store brand" drugs
respectively, and Synovics Labs, Inc. a drug development subsidiary
that is pursuing generic drug opportunities. Synovics employs
approximately 150 people in its Ft. Lauderdale facility of 80,000.
Sq Ft. The Company manufactures drug products in specialized
containment suites including hormonal prescription drugs and under
its Drug Enforcement Administration licenses. The Company has a
Front-End strategy based business plan -- a strategy of sourcing
lowest cost, highly competitive generic drug products from India,
marketed to its US customer through its Ft. Lauderdale operations.
Synovics' previously announced strategic partnerships with Maneesh
Pharmaceuticals, LTD and Harcharan (Harry) Singh of Glopec
International that represent the Company's cornerstone for its
Front-End strategy in India. The Company believes cost is the
single most important element in the generic drug industry and it
is reaching out through its strategic partners to source products
and services from a variety of smaller and quite willing
independent Indian pharmaceutical companies that have these assets,
but also have limited means of accessing the US market. "Safe
Harbor" statements under the Private Securities Litigation Reform
Act of 1995: Except for the historical information contained
herein, the statements made in this press release constitute
forward-looking statements within the meaning of Section 27A of the
Securities Act of 1933 and Section 21E of the Securities Exchange
Act of 1934. Forward-looking statements can be identified by their
use of words such as "expects," "plans" "projects," "will," "may,"
"anticipates," "believes," "should," "intends," "estimates" and
other words of similar meaning. Because such statements inherently
involve risks and uncertainties that cannot be predicted or
quantified, actual results may differ materially from those
expressed or implied by such forward-looking statements depending
upon a number of factors affecting the Company's business. These
factors include, among others: the difficulty in predicting the
timing and outcome of product development including biostudies
demonstrating "bioequivalency," outcome of any pending or potential
legal proceedings including an undertaking to recover common stock
held in escrow; any patent-related matters such as patent challenge
settlements and patent infringement cases; the outcome of
litigation arising from challenging the validity or
non-infringement of patents covering its products; the difficulty
of predicting the timing of FDA approvals; court and FDA decisions
on exclusivity periods; the ability of competitors to extend
exclusivity periods for their products; the Company's ability to
complete product development activities in the timeframes and for
the costs it expects; market and customer acceptance and demand for
its products; the Company's possible dependence on revenues from
significant customers; the use of estimates in the preparation of
the Company's financial statements; the potential for competitors
to file ANDAs prior to any filing by the Company pertaining to the
same target brand; the impact of competitive products and pricing
on products, including the launch of authorized generics; the
ability to launch new products in the timeframes it expects; the
availability of raw materials; the availability of any product it
may purchase; the regulatory environment; the Company's exposure to
product liability and other lawsuits and contingencies; the
increasing cost of insurance and the availability of product
liability insurance coverage; the Company's timely and successful
completion of strategic initiatives, including integrating
companies and products it may acquire and implementing its
Front-End India strategy; fluctuations in operating results,
including the effects on such results from spending for research
and development, sales and marketing activities and patent
challenge activities; the inherent uncertainty associated with
financial projections; the outcome of ongoing efforts to improve
Kirks operational efficiency and customer performance; changes in
generally accepted accounting principles, fluctuations in operating
results; capital adequacy; statements of future plans relating to
the Company's capital needs, product development and filings with
the FDA, viability, application or continuation of the Company's
business licenses including Drug, Enforcement and Administrations
licenses for scheduled drugs; business and growth strategies;
statements specifically concerning the successful closing of
acquisitions, and satisfying closing conditions of any current or
future financial transactions including debt or equity
requirements, regulatory requirements; and meeting conditions set
by potential equity investors, reliance on key strategic alliances,
capital markets, and in general risks related to the regulatory
environment and government approval processes, and any other risks
detailed from time to time in the Company's filings with the
Securities and Exchange Commission. The forward-looking statements
contained in this press release speak only as of the date the
statement was made. The Company undertakes no obligation (nor does
it intend) to publicly update or revise any forward-looking
statements, whether as a result of new information, future events
or otherwise, except to the extent required under applicable law.
DATASOURCE: Synovics Pharmaceuticals, Inc. CONTACT: Ronald Howard
Lane, Ph.D., of Synovics Pharmaceuticals, Inc., Chairman and CEO,
+1-954-486-4590 Web site: http://www.synovics.com/
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