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

 

December 5, 2012

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))

 

 
 

 

Item 1.01 Entry into a Material Definitive Agreement.

 

Bridge Loan Agreement

 

On December 5, 2012 (the “Effective Date”), Elite Pharmaceuticals, Inc. (the “Company”) amended its bridge loan agreement (the “Loan Agreement”) with Jerry Treppel, the Company’s Chairman and CEO pursuant to which it increased the maximum principal amount that the Company can draw under the Loan Agreement (“Credit Line”) from $500,000 to $1,000,000. All other terms remain the same. Mr. Treppel provided the increased Credit Line for the purpose of providing working capital to support Elite’s increase in production and growth of sales.

 

On December 10, 2012, the Company issued a press release announcing that it had amended the Loan Agreement. A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated by reference herein.

 

Item 9.01                      Financial Statements and Exhibits

 

d)     Exhibits

 

Exhibit No.   Exhibit Description
     
10.1   Amendment to Loan Agreement dated December 5, 2012
     
99.1   Press Release dated December 10, 2012

 

2
 

 

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: December 10, 2012

 

  ELITE PHARMACEUTICALS, INC.
     
  By: /s/ Chris Dick
    Chris Dick, President &
    Chief Operating Officer

 

3

 

 

EXHIBIT 10.1

 

Amendment No. 1 to

Treppel Loan Agreement

 

WHEREAS, Elite Pharmaceuticals, Inc., a Nevada corporation (the “ Borrower ”), and Jerry Treppel, a resident of New Jersey (the “ Lender ”) entered into that certain Loan Agreement dated December 5, 2012 (the “ Agreement ”); and

 

WHEREAS, Lender and Borrower desire to amend the Agreement to increase the maximum principal amount of the Credit Line (as defined in the Agreement) from $500,000 to $1,000,000; and

 

WHEREAS, pursuant to Section 7.5 of the Agreement the Agreement can be amended provided such amendment is in writing and executed by the Lender and the Borrower.

 

NOW THEREFORE, in consideration of the premises, the mutual provisions contained in the Agreement, and other good and valuable consideration the receipt and adequacy of which are hereby acknowledged, the Borrower and Lender agree as follows:

 

1. The maximum principal amount of the Credit Line (as defined in the Agreement) is hereby increased from $500,000 to $1,000,000.
2. The Promissory Note issued in conjunction with the Agreement is superseded and replaced with the New Promissory Note, a copy of which is attached hereto.
3. Except as otherwise expressly provided herein, the Agreement and the obligations of the Borrower thereunder, and each of the rights of and benefits to the Borrower thereunder is, and shall continue to be, in full force and effect and each is hereby ratified and confirmed in all respects.
4. This Amendment may be executed in two or more identical counterparts, all of which shall be considered one and the same agreement and shall become effective when counterparts have been signed by each party and delivered to the other party. In the event that any signature is delivered by facsimile transmission or by an e-mail which contains a portable document format (.pdf) file of an executed signature page, such signature page shall create a valid and binding obligation of the party executing (or on whose behalf such signature is executed) with the same force and effect as if such signature page were an original thereof.

 

[ signature page follows ]

 

 
 

 

IN WITNESS WHEREOF, the Borrower and Lender have caused their respective signature page to this Amendment to be duly executed as of the 5th day of December, 2012.

 

  ELITE PHARMACEUTICALS, INC.    
         
  By: /s/ Chris Dick   /s/ Jerry Treppel
    Chris Dick, President   Jerry Treppel

 

 

 

 

EXHIBIT 99.1

 

Z:/TQDATA/VINEYARD/LIVE JOBS/2012/12 DEC/07 DEC/SHIFT III/ELITE PHARMA/DRAFT/03-PRODUCTION

 

ELITE PHARMACEUTICALS ANNOUNCES AMENDMENT TO BRIDGE LOAN FACILITY

 

NORTHVALE, N.J. – December 10, 2012 – Elite Pharmaceuticals, Inc. ("Elite”) (OTCBB: ELTP) announced today that it has amended the bridge loan agreement (“Loan Agreement”) with Jerry Treppel, Elite’s Chairman & CEO. Pursuant to the amendment to the Loan Agreement, Mr. Treppel has agreed to increase the maximum principal amount of the line of credit from $500,000 to $1,000,000. All other terms remain the same. The additional proceeds will be used primarily for working capital to support Elite’s increase in production and growth of sales.

 

A copy of the amendment to the Loan Agreement will be filed in a Current Report on Form 8-K which will be filed with the Securities and Exchange Commission.

 

About Elite Pharmaceuticals, Inc.

 

Elite Pharmaceuticals, Inc. develops oral sustained and controlled release products. Elite's strategy includes assisting partner companies in the life cycle management of products to improve off-patent drug products and developing generic versions of controlled release drug products with high barriers to entry. Elite has three commercial products being sold through a partner, two products produced for partners under contract manufacturing agreements, two additional products approved and pending launch, and two products under review, pending approval by the FDA. Elite’s lead pipeline products include abuse resistant opioids utilizing the company’s patented proprietary technology, and a once-daily opioid. They are sustained release oral formulations of opioids for the treatment of chronic pain, which address two of the limitations of existing oral opioids: the provision of consistent relief of baseline pain levels and deterrence of potential abuse. Elite also has partnered with Mikah Pharma to develop a new product, with Hi-Tech Pharmacal to develop an intermediate for a generic product, and a Hong Kong based company to develop a branded product for the United States market and its territories. Elite operates a GMP and DEA registered facility for research, development, and manufacturing located in Northvale, NJ.

  

This news release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Including 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 risks and uncertainties including, without limitation, delays, uncertainties, inability to obtain necessary ingredients and other factors not under the control of Elite 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 risks and other factors, including, without limitation, the timing or results of pending and future clinical trials, regulatory reviews and approvals by the Food and Drug Administration and other regulatory authorities, intellectual property protections and defenses, and the Company’s ability to operate as a going concern, are discussed in Elite's filings with the Securities and Exchange Commission, including its reports on forms 10-K, 10-Q and 8-K. Elite undertakes no obligation to update any forward-looking statements.

 

Contact:

Elite Pharmaceuticals, Inc.

Dianne Will, Investor Relations, 518-398-6222

Dianne@elitepharma.com