Amneal Receives U.S. FDA Approval for Potassium Phosphates Injection IV Bags
29 Luglio 2024 - 10:05PM
Business Wire
First presentation of preservative-free
potassium phosphates in a single-dose IV infusion bag
Third 505(b)(2) injectable added this year –
will launch in third quarter
Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX) (“Amneal” or the
“Company”) today announced that it has received New Drug
Application (“NDA”) approval from the U.S. Food and Drug
Administration (FDA) for its new presentation of potassium
phosphates in 0.9% sodium chloride injection intravenous (IV)
ready-to-use (RTU) bags. This sterile presentation reduces the
compounding steps for clinicians typically required with
administering the product.
Potassium Phosphates in Sodium Chloride Injection is a
phosphorus replacement product indicated as a source of phosphorus
to correct hypophosphatemia in adults and pediatric patients who
weigh 40 kg or greater when oral or enteral replacement is not
possible, insufficient or contraindicated. The product is available
as a single-dose infusion bag and is formulated without
preservatives. It is natural rubber latex-free and can be stored at
room temperature.
In 2024, Amneal has already launched PEMRYDI RTU®, a
ready-to-use formulation of pemetrexed, and FOCINVEZ®, a
ready-to-use version of fosaprepitant. Both products offer
hospitals and oncology clinics new, value-added presentations that
should improve pharmacy efficiency by eliminating preparation
steps. The expected third quarter launch of potassium phosphates
injection IV bag represents the Company’s third 505(b)(2) launch
this year.
“We are pleased to offer this new differentiated injectable
product to hospitals,” said Andy Boyer, Executive Vice President,
Chief Commercial Officer - Generics. “This new IV parenteral
infusion bag is preservative-free and can be stored at room
temperature. With the addition of new 505(b)(2) injectables, we are
meaningfully expanding our injectables portfolio.”
"Our third 505(b)(2) injectable product approval this year
reflects our deep capabilities in developing new and impactful
complex products. We look forward to bringing more innovative
505(b)(2) injectable products to market over the coming years,"
said Dr. Srinivas Kone, Senior Vice President, Chief Scientific
Officer – Generics.
Adverse effects reported for the potassium phosphates injection
IV bags include hyperkalemia, hyperphosphatemia, hypocalcemia and
hypomagnesemia. For full prescribing information, see package
insert located here.
About Amneal
Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX), headquartered in
Bridgewater, NJ, is a global pharmaceutical 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.
Cautionary Statement on Forward-Looking Statements
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
management’s intentions, plans, beliefs, expectations, financial
results, or forecasts for the future, including among other things:
discussions of future operations; expected or estimated operating
results and financial performance; and statements regarding our
positioning, including our ability to drive sustainable long-term
growth, and other non-historical statements. Words such as “plans,”
“expects,” “will,” “anticipates,” “estimates,” and similar words,
or the negatives thereof, are intended to identify estimates and
forward-looking statements.
The reader is cautioned not to rely on these forward-looking
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, including recent events affecting the
financial services industry; 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.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240729345025/en/
Investor Contact Anthony DiMeo VP, Investor Relations
& Media anthony.dimeo@amneal.com
Grafico Azioni Amneal Pharmaceuticals (NYSE:AMRX)
Storico
Da Ott 2024 a Nov 2024
Grafico Azioni Amneal Pharmaceuticals (NYSE:AMRX)
Storico
Da Nov 2023 a Nov 2024