Elite Pharmaceuticals

Those following the progress of Elite Pharmaceuticals, Inc. (OTCBB: ELTP) have seen the latest announcement of the US Food and Drug Administration’s (FDA) acceptance for review of an Abbreviated New Drug Application (ANDA) on December 21, 2023, for an undisclosed generic drug product in a class of medications known as central nervous stimulants. 

More importantly, Elite Pharmaceuticals, Inc. (OTCBB: ELTP) has seen increased trading in the past few weeks.

Elite Pharmaceuticals, Inc. is a specialty pharmaceutical company developing, manufacturing, and distributing 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 and 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 in Northvale, NJ. For more information, visit www.elitepharma.com.

This trading opportunity in the specialty pharmaceutical industry is moving forward and should immediately add (ELTP) to their watch list.

Recent News:

Elite Pharmaceuticals Files ANDA with US FDA to Market Central Nervous System Stimulant

NORTHVALE, NJ / ACCESSWIRE / December 26, 2023 / Elite Pharmaceuticals, Inc. (“Elite” or the “Company”) (OTCBB:ELTP), a specialty pharmaceutical company engaged in the development, manufacture, and distribution of niche generic products, today announced the US Food and Drug Administration’s (FDA) acceptance for review of an Abbreviated New Drug Application (ANDA) on December 21, 2023, for an undisclosed generic drug product in a class of medications known as central nervous stimulants. IQVIA reported annual sales for the twelve months ending June 2023 of $5.1 billion for the brand and generic market for this product.

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.

Elite Pharmaceuticals, Inc. is a specialty pharmaceutical company engaged in the development and manufacture of oral, controlled-release products, using proprietary know-how and technology for the manufacture of generic pharmaceuticals.

Our strategy includes developing generic versions of controlled-release drug products with high-barriers to entry.

Elite owns multiple generic products, some of which are licensed to Prasco, LLC and TAGI Pharma.

Elite operates a cGMP and DEA registered facility for research, development, and manufacturing located in Northvale, NJ.

GENERIC PIPELINE

Elite is developing differentiated niche generic products for future growth. Elite’s focus is on solid oral dose products that are hard to formulate, such as extended-release products and products that we believe have competitive advantages. Elite also continues to evaluate contract development, contract manufacturing, and in-licensing opportunities. Updates on development projects will be provided upon achieving key milestones.

The Barchart Technical Opinion rating is a 100% Buy and ranks in the Top 1% of all short term signal directions.

Start your research on ELTP now. 

UPDATES TO FOLLOW….

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