Amneal Expands Broad Injectables Portfolio to Over 40 Products with the Addition of Six New Therapies
05 Juin 2024 - 2:00PM
Business Wire
The Company’s leading R&D capabilities and robust, expanded
manufacturing capacity are helping to address chronic market
shortages
Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX) (“Amneal” or the
“Company”) today announced the continued expansion of its
injectables portfolio with six new injectable product launches
during the second quarter of 2024, bringing the Company’s total
number of commercial injectable products available for the U.S.
institutional market to over 40.
The growth of Amneal’s broad injectables portfolio will help
address shortages of critical products where there may be little or
no clinical alternative, including in key categories such as
oncology. The American Society of Health System Pharmacists (ASHP)
currently lists 323 active U.S. drug shortages, with about half
representing injectables.
Notably, three of Amneal’s six new injectable products are
currently on the ASHP drug shortage list. With these new launches,
Amneal now provides 13 injectables that are on the ASHP shortage
list.
Amneal’s Q2 2024 injectable product launches:
Product launch
Dosage form
ASHP drug shortage
1
PEMRYDI RTU®
Vial
No
2
Atropine sulfate
Prefilled syringe
Yes
3
Docetaxel
Injection
Yes
4
Foscarnet
IV bag
No
5
Methylprednisolone acetate
Multi-dose vial
Yes
6
Calcium gluconate
Vial
No
“The persistent shortage of quality injectables is driven by
multiple factors, including unstable market economics, supply chain
disruptions and the need for supply redundancy. Amneal has made
meaningful investments to expand our capacity and capabilities and
deliver on our goal to be a significant injectables player.
Importantly, we are building a robust portfolio of injectables that
can serve as a reliable solution to market shortages. We are
focused on being a partner our customers can count on to provide a
consistent supply of high-quality medicines for their patients,”
said Andy Boyer, Executive Vice President, Chief Commercial Officer
– Generics.
Amneal has tripled its injectables capacity to 60 million units
across four manufacturing facilities over the past few years and
expects to have over 60 commercial injectable products in 2025. In
particular, the Company is launching branded oncology 505(b)(2)
products such as PEMRYDI RTU®. These injectables are new,
ready-to-use presentations that can improve pharmacy efficiency by
reducing clinician steps. Amneal expects to launch two to three new
505(b)(2) injectables per year going forward.
About Amneal
Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX), headquartered in
Bridgewater, NJ, is a global pharmaceuticals company. We make
healthy possible through the development, manufacturing, and
distribution of a diverse portfolio of over 280 pharmaceutical
products, primarily within the United States. In its Generics
segment, the Company is expanding across a broad range of complex
product categories and therapeutic areas, including injectables and
biosimilars. In its Specialty segment, Amneal has a growing
portfolio of branded pharmaceuticals focused primarily on central
nervous system and endocrine disorders, with a pipeline focused on
unmet needs. Through its AvKARE segment, the Company is a
distributor of pharmaceuticals and other products for the U.S.
federal government, retail, and institutional markets. For more
information, please visit www.amneal.com.
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Certain statements contained herein, regarding matters that are
not historical facts, may be forward-looking statements (as defined
in the U.S. Private Securities Litigation Reform Act of 1995). Such
forward-looking statements include statements regarding
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statements. These forward-looking statements are based on current
expectations of future events, including with respect to future
market conditions, company performance and financial results,
operational investments, business prospects, new strategies and
growth initiatives, the competitive environment, and other events.
If the underlying assumptions prove inaccurate or known or unknown
risks or uncertainties materialize, actual results could vary
materially from the expectations and projections of the Company.
Such risks and uncertainties include, but are not limited to: our
ability to successfully develop, license, acquire and commercialize
new products on a timely basis; the competition we face in the
pharmaceutical industry from brand and generic drug product
companies, and the impact of that competition on our ability to set
prices; our ability to obtain exclusive marketing rights for our
products; our revenues are derived from the sales of a limited
number of products, a substantial portion of which are through a
limited number of customers; the impact of a prolonged business
interruption within our supply chain; the continuing trend of
consolidation of certain customer groups; our dependence on
third-party suppliers and distributors for raw materials for our
products and certain finished goods; legal, regulatory and
legislative efforts by our brand competitors to deter competition
from our generic alternatives; our dependence on information
technology systems and infrastructure and the potential for
cybersecurity incidents; our ability to attract, hire and retain
highly skilled personnel; risks related to federal regulation of
arrangements between manufacturers of branded and generic products;
our reliance on certain licenses to proprietary technologies from
time to time; the significant amount of resources we expend on
research and development; the risk of claims brought against us by
third parties; risks related to changes in the regulatory
environment, including U.S. federal and state laws related to
healthcare fraud abuse and health information privacy and security
and changes in such laws; changes to Food and Drug Administration
product approval requirements; the impact of healthcare reform and
changes in coverage and reimbursement levels by governmental
authorities and other third-party payers; our dependence on
third-party agreements for a portion of our product offerings; our
substantial amount of indebtedness and our ability to generate
sufficient cash to service our indebtedness in the future, and the
impact of interest rate fluctuations on such indebtedness; our
potential expansion into additional international markets
subjecting us to increased regulatory, economic, social and
political uncertainties; our ability to identify, make and
integrate acquisitions or investments in complementary businesses
and products on advantageous terms; the impact of global economic,
political or other catastrophic events; our obligations under a tax
receivable agreement may be significant; and the high concentration
of ownership of our Class A common stock and the fact that we are
controlled by the Amneal Group. The forward-looking statements
contained herein are also subject generally to other risks and
uncertainties that are described from time to time in the Company’s
filings with the Securities and Exchange Commission, including
under Item 1A, “Risk Factors” in the Company’s most recent Annual
Report on Form 10-K and in its subsequent reports on Forms 10-Q and
8-K. Investors are cautioned not to place undue reliance on any
such forward-looking statements, which speak only as of the date
they are made. Forward-looking statements included herein speak
only as of the date hereof and we undertake no obligation to revise
or update such statements to reflect the occurrence of events or
circumstances after the date hereof.
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version on businesswire.com: https://www.businesswire.com/news/home/20240605270382/en/
Contact Anthony DiMeo VP, Investor Relations & Media
anthony.dimeo@amneal.com
Amneal Pharmaceuticals (NYSE:AMRX)
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