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Sep 23, 2003
Elite Pharmaceuticals Announces Revised Exchange Offer
Northvale, New Jersey, Tuesday, September 23, 2003: Elite Pharmaceuticals, Inc. (“Elite” or the “Company”) (AMEX: ELI) which develops generic and brand-name oral pharmaceuticals applicable to delayed, sustained, targeted and pulsatile release tablets and capsules, announced today that it’s Board of Directors has authorized an offer to exchange its Class C Warrants for previously issued Class A Warrants which expired on November 30, 2002 without requiring a payment of an exchange fee of $0.10 per warrant. The latter requirement had been pursuant to a previously announced settlement agreement with a group of holders of the Company’s Common Stock and Class A Warrants.

The effect of the exchange offer is to extend the expiration date of the Class A Warrants from November 30, 2002 to November 30, 2005, and reduce the exercise price from $6.00 to $5.00. The Class C Warrants are non-transferrable.

The holders of the Class A Warrants can receive the Class C Warrants by surrendering or having their brokers’ surrender their Class A Warrants to Company’s transfer agent, New Jersey Transfer and Trust Company.

There are currently 1,721,179 Class A Warrants outstanding, all of which are entitled to exchange for the Class C Warrants. The Company plans to file a registration statement, with the Securities Exchange Commission to register the shares of the Company’s Common Stock issuable upon exercise of the Class C Warrants. The offer, absent the exchange fee, shows our commitment to those who were involved in the Company's past financing efforts," says Bernard Berk, CEO of Elite.

About Elite Pharmaceuticals
Elite Pharmaceuticals is a specialty pharmaceutical company principally engaged in the development of oral, controlled release (CR) products. Elite develops CR products internally and licenses CR products using its proprietary technology. The Company’s strategy includes developing CR versions of generic drugs with high barriers to entry and assisting in the life cycle management of products to improve off patent drugs. Elite’s technology is applicable to develop delayed, sustained or targeted release pellets, capsules, tablets, granules and powders for NDA or ANDA submission. Elite has a pipeline of six products under development in the therapeutic areas that include cardiovascular, pain, allergy and infection. Elite also has a GMP and DEA approved facility for commercial scale manufacturing in Northvale, NJ.

FOR FURTHER INFORMATION, CONTACT:
For Elite Pharmaceuticals, Inc.
Dianne Will
Investor Relations
518-398-6222
dwill@willstar.net

This release contains forward-looking statements which involve known and unknown risks, delays, uncertainties and other factors not under the Company's control, which may cause actual results, performance or achievements of the Company to be materially different from the results, performance or other expectations implied by these forward-looking statements. These factors include results of current or pending research and development activities, actions by the FDA and other regulatory authorities, and those factors detailed in the Company's filings with the Securities and Exchange Commission such as 10K, 10Q and 8K reports.