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ELITE PHARMACEUTICALS INC /NV/
0001053369
2024-10-10
2024-10-10
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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
WASHINGTON,
D.C. 20549
FORM
8-K
CURRENT
REPORT
PURSUANT
TO SECTION 13 OR 15(D)
OF
THE SECURITIES EXCHANGE ACT OF 1934
October
10, 2024
Date
of Report (Date of earliest event reported)
ELITE
PHARMACEUTICALS, INC.
(Exact
name of registrant as specified in its charter)
Nevada |
|
001-15697 |
|
22-3542636 |
(State
or other jurisdiction |
|
(Commission |
|
(IRS
Employer |
of
incorporation) |
|
File
Number) |
|
Identification
No.) |
165
Ludlow Avenue, Northvale, New Jersey 07647
(Address
of principal executive offices)
(201)
750-2646
(Registrant’s
telephone number, including area code)
(Former
name or former address, if changed since last report.)
Check
the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under
any of the following provisions:
☐ |
Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|
|
☐ |
Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Indicate
by check mark whether the registrant is an emerging growth company as defined in as defined in Rule 405 of the Securities Act of 1933
(§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company ☐
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of each exchange on which registered |
Common
Stock, par value $0.001 per share |
|
ELTP |
|
OTCQB |
Item
7.01 Regulation FD Disclosure.
On
October 10, 2024, Elite Pharmaceuticals Inc. (“Elite”) announced the Israeli Ministry of Health approval for Elite’s
generic version of Adderall®, an immediate-release mixed salt of a single entity Amphetamine product (Dextroamphetamine Saccharate,
Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate) with strengths of 10 mg, 20 mg, and 30 mg tablets on October 7,
2024.
Elite
will supply the product to Dexcel Pharma (Or Akiva, Israel), the Company’s exclusive distributor, for the Israeli market. The product
is a central nervous system stimulant and is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) and Narcolepsy.
Under
the License and Distribution Agreement with Dexcel, Elite
will manufacture and package the generic product under Dexcel’s label. Dexcel will provide sales, marketing, and distribution at
its expense. Dexcel will pay an agreed upon transfer price for the product and share profits under certain conditions. Elite’s
generic Adderall® product is jointly owned by Elite and Mikah Pharma LLC. The first shipment is dependent on the timing of licensee
orders, DEA quotas and manufacturing which could take months.
A
copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K. The information set forth in this Item 7.01
and contained in the press release furnished as Exhibit 99.1 shall not be deemed “filed” for purposes of Section 18 of the
Securities Exchange Act of 1934, as amended, or the Exchange Act, and is not incorporated by reference into any of Elite’s filings
under the Securities Act of 1933, as amended, or the Securities Act, or the Exchange Act, whether made before or after the date hereof,
except as shall be expressly set forth by specific reference in any such filing.
Item
9.01 Financial Statements and Exhibits.
(d)
Exhibits.
SIGNATURE
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by
the undersigned hereunto duly authorized.
Dated:
October 10, 2024 |
ELITE
PHARMACEUTICALS, INC. |
|
|
|
By: |
/s/
Nasrat Hakim |
|
|
Nasrat
Hakim, President and CEO |
Exhibit
99.1
Elite
Pharmaceuticals’ Generic Adderall® Receives Marketing Approval from the Israeli Ministry of Health
NORTHVALE,
N.J. – October 10, 2024 – Elite Pharmaceuticals, Inc. (“Elite” or the “Company”) (OTCQB: ELTP), a
specialty pharmaceutical company developing niche generic products, today announced the Israeli Ministry of Health approval for Elite’s
generic version of Adderall®, an immediate-release mixed salt of a single entity Amphetamine product (Dextroamphetamine
Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate) with strengths of 10 mg, 20 mg, and 30 mg tablets.
Elite will supply the product to Dexcel Pharma (Or Akiva, Israel), the Company’s exclusive distributor, for the Israeli market.
The product is a central nervous system stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) and
Narcolepsy.
Under
the License and Distribution Agreement with Dexcel, Elite
will manufacture and package the generic product under Dexcel’s label. Dexcel will provide sales, marketing, and distribution at
its expense. Dexcel will pay an agreed upon transfer price for the product and share profits under certain conditions. Elite’s
generic Adderall® product is jointly owned by Elite and Mikah Pharma LLC. The first shipment is dependent on the timing
of licensee orders, DEA quotas and manufacturing, which could take months.
About
Elite Pharmaceuticals, Inc.
Elite
Pharmaceuticals, Inc. is a specialty pharmaceutical company that develops, manufactures, and distributes niche generic products. Elite’s
product lines consist of immediate-release and controlled-release, solid oral dose products, which are marketed under the Elite Laboratories
label, as well as pursuant to licenses granted to third-party pharmaceutical marketing and distribution organizations. Elite operates
a cGMP and DEA registered facility for research, development, and manufacturing located in Northvale, NJ. For more information, visit
www.elitepharma.com.
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act
of 1995, including, without limitation, those related to the effects, if any, on future results, performance or other expectations that
may have some correlation to the subject matter of this press release. Readers are cautioned that such forward-looking statements involve,
without limitation, risks, uncertainties, and other factors not under the control of Elite, which may cause actual results, performance
or achievements of Elite to be materially different from the results, performance or other expectations that may be implied by these
forward-looking statements. These forward-looking statements may include statements regarding the expected timing of approval, if at
all, of products by the FDA and the actions the FDA may require of Elite in order to obtain such approvals. These forward-looking statements
are not guarantees of future action or performance. These risks and other factors are discussed, without limitation, in Elite’s
filings with the Securities and Exchange Commission, including its reports on forms 10-K, 10-Q, and 8-K. Elite is under no obligation
to update or alter its forward-looking statements, whether as a result of new information, future events or otherwise.
Contact:
Elite
Pharmaceuticals, Inc.
Dianne
Will, Investor Relations
518-398-6222
Dianne@elitepharma.com
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