ELTP on OTC

ELITE PHARMACEUTICALS INC /NV/

ELITE PHARMACEUTICALS INC /NV/ is an American pharmaceutical preparations company, incorporated in New Jersey.1 It is headquartered in Northvale, New Jersey.1 Its shares trade on OTC under the symbol ELTP.1

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Last updated Oct 20, 2026.

Overview

$148.9MRevenue, fiscal 20262
$44.9MNet income, fiscal 20262

Compare with Clovis Oncology, MACROGENICS INC or Karyopharm Therapeutics Inc., or pick any stock.

  • TickerELTP on OTC1
  • IndustryPharmaceutical Preparations1
  • HeadquartersNorthvale, New Jersey1
  • Incorporated inNJ3
  • Business address165 Ludlow Avenue, Northvale, Nj 076473
  • Filer categoryNon-accelerated filer, Smaller reporting company3

Act of 1984 (the “Drug Price Competition Act”) as well as generic drug products which require ANDAs.4 From its latest annual report

Financials

From the company’s reports to the SEC. Every number links to the filing it came from.

Key numbers, fiscal 2026

50.4%Gross margin2
33.0%Operating margin2
30.1%Net margin2
77.1%Revenue growth, 20262
45.4%Return on equity2
$22.8MFree cash flow2

What sells

Revenue by product, business segment and region, as the company reports it to the SEC.

Products and services

Scheduled Products Manufacturing Fees brought in 48% of the revenue ELITE PHARMACEUTICALS INC /NV/ broke down this way in fiscal 2026.

  1. Scheduled Products Manufacturing Fees$141.5M248%up 89% from 2025
  2. Indirect Sales to Wholesalers$82.5M228%up 143% from 2025
  3. Direct Sales to Wholesalers$65.3M222%up 36% from 2025
  4. Unscheduled Products Manufacturing Fees$6.3M22%down 12% from 2025
  5. Unscheduled Products Licensing Fees$594.5K20%down 67% from 2025
  6. Scheduled Products Licensing Fees$465.5K20%up 87% from 2025
Products and services by year
Products and services20252026
Scheduled Products Manufacturing Fees$74.8M$141.5M
Indirect Sales to Wholesalers$34.0M$82.5M
Direct Sales to Wholesalers$48.0M$65.3M
Unscheduled Products Manufacturing Fees$7.2M$6.3M
Unscheduled Products Licensing Fees$1.8M$594.5K
Scheduled Products Licensing Fees$248.8K$465.5K

Where the money goes

Where each dollar of revenue went, fiscal 2026

  • Cost of revenue50¢$73.8M
  • Research and development4¢$5.7M
  • Other costs8¢$12.5M
  • Income tax8¢$11.9M
  • Profit30¢$44.9M

Out of $148.9M in revenue.2

Where each dollar of operating cash went, fiscal 2026

  • Capital spending4¢$925.6K
  • Kept or used elsewhere96¢$22.8M

Out of $23.7M of cash from operations.2

Financial statements

Revenue56789102$148.9M in 2026+1867% since 2019
0$50.0M$100.0M$150.0M2019: $7.6M$7.6M20192020: $18.0M$18.0M2020+138%2021: $25.4M$25.4M2021+41%2022: $32.3M$32.3M2022+27%2023: $34.2M$34.2M2023+6%2024: $56.6M$56.6M2024+66%2025: $84.0M$84.0M2025+48%2026: $148.9M$148.9M2026+77%
Gross profit56789102$75.0M in 2026+2516% since 2019
0$20.0M$40.0M$60.0M$80.0M2019: $2.9M$2.9M20192020: $8.0M$8.0M2020+178%2021: $11.9M$11.9M2021+49%2022: $14.8M$14.8M2022+25%2023: $16.6M$16.6M2023+12%2024: $26.4M$26.4M2024+59%2025: $40.1M$40.1M2025+52%2026: $75.0M$75.0M2026+87%
Operating income56789102$49.1M in 2026
-$20.0M0$20.0M$40.0M$60.0M2019: -$9.2M-$9.2M20192020: -$2.3M-$2.3M2020−75%2021: $2.1M$2.1M20212022: $5.1M$5.1M2022+141%2023: $3.7M$3.7M2023−28%2024: $10.8M$10.8M2024+193%2025: $19.6M$19.6M2025+82%2026: $49.1M$49.1M2026+151%
Net income56789102$44.9M in 2026
-$20.0M0$20.0M$40.0M$60.0M2019: -$9.3M-$9.3M20192020: -$2.2M-$2.2M2020−76%2021: $5.1M$5.1M20212022: $8.9M$8.9M2022+75%2023: $3.6M$3.6M2023−60%2024: $20.1M$20.1M2024+465%2025: -$4.3M-$4.3M20252026: $44.9M$44.9M2026

Every line of the income statement as filed: the last 2 fiscal years, latest first.2

Period ending2026-03-312025-03-31
Total revenue$148.9M$84.0M
Cost of manufacturing$73.8M$44.0M
Gross profit$75.0M$40.1M
Research and development$5.7M$8.0M
General and administrative$17.6M$9.0M
Non-cash compensation through issuance of stock options$176.5K$227.6K
Impairment of intangible assets$847.0K$1.6M
Depreciation and amortization$1.5M$1.7M
Total operating expenses$25.9M$20.5M
Income from operations$49.1M$19.6M
Change in fair value of derivative financial instruments - warrants$7.9M-$18.9M
Interest expense and amortization of debt issuance costs-$396.7K-$772.4K
Interest income$207.9K$20.9K
Other income$34.5K
Other income (expense), net$7.7M-$19.7M
Income (loss) before income taxes$56.8M-$52.1K
Income tax expense-$11.9M-$4.3M
Net income (loss)$44.9M-$4.3M
Basic net income (loss) per share$0.04$0.00
Diluted net income (loss) per share$0.03$0.00
Basic weighted average common stock outstanding1.1B shares1.1B shares
Diluted weighted average common stock outstanding1.1B shares1.1B shares

Compare ELITE PHARMACEUTICALS INC /NV/ with another company

What it owns

What ELITE PHARMACEUTICALS INC /NV/ reports owning in its annual reports to the SEC: buildings, land and equipment, real estate and locations, investments, intangible assets and inventory, at the end of its latest fiscal year and a year before.

Property and equipment

ItemLatestA year beforeChange
Property and equipment, before depreciation$28.3M2 Mar 31, 2026$27.4M2 Mar 31, 2025+3.4%
Accumulated depreciation$18.1M2 Mar 31, 2026$17.0M2 Mar 31, 2025+6.3%
Property and equipment, net$10.2M2 Mar 31, 2026$10.3M2 Mar 31, 2025−1.4%
Finance-lease assets$1.3M2 Mar 31, 2026$1.8M2 Mar 31, 2025−26.9%
Operating-lease assets (leased space)$1.5M2 Mar 31, 2026$2.0M2 Mar 31, 2025−23.5%

Intangibles and goodwill

ItemLatestA year beforeChange
Finite-lived intangibles, gross$5.6M2 Mar 31, 2026$6.3M2 Mar 31, 2025−11.1%
Finite-lived intangibles, net$4.8M2 Mar 31, 2026$5.6M2 Mar 31, 2025−15.0%

Inventory

ItemLatestA year beforeChange
Inventory, total$21.3M2 Mar 31, 2026$16.2M2 Mar 31, 2025+30.9%
Raw materials$12.6M2 Mar 31, 2026$10.0M2 Mar 31, 2025+26.0%
Work in process$3.3M2 Mar 31, 2026$1.4M2 Mar 31, 2025+129.8%
Finished goods$5.4M2 Mar 31, 2026$4.8M2 Mar 31, 2025+11.9%

Properties, in its own words

We own a facility located at 165 Ludlow Avenue, Northvale, New Jersey (“165 Ludlow”) which contains approximately 15,000 square feet of floor space. This real property and the improvements thereon are encumbered by a mortgage in favor of the New Jersey Economic Development Authority (“NJEDA”) as security for a loan through tax-exempt bonds from the NJEDA to Elite. The mortgage contains certain customary provisions including, without limitation, the right of NJEDA to foreclose upon a default by Elite. The NJEDA has declared the payment of this bond to be in default (for more information on the NJEDA Bonds, see Part II, Item 7 “Management’s Discussion and Analysis of Financial Condition and Results of Operations; Liquidity and Capital Resources; NJEDA Bonds”). We are currently using the facility as a laboratory, manufacturing, storage, distribution, and office space.

We own a facility located at 135-137 Ludlow Avenue, Northvale, New Jersey (“135 Ludlow”) which contains approximately 35,000 square feet of floor space. This real property and the improvements thereon are encumbered by a mortgage in favor of East West Bank.

The rest of Item 2

In October 2020, the Company entered into an operating lease for office space in Pompano Beach, Florida (the “Pompano Office Lease”). The Pompano Office Lease is for approximately 1,275 square feet of office space, with Elite taking occupancy on November 1, 2020. The Pompano Office includes a three month abatement from November 2020 through February 2021 and had an original term of three years, ending on October 31, 2023. The Pompano Office Lease was extended for one additional year to October 31, 2024. The Pompano Office Lease expired on October 31, 2024.

In October 2024, the Company entered into an operating lease for office space in Pompano Beach, Florida, at a different location than the property related to the Pompano Office Lease (the “Pompano Office 2 Lease”). The Pompano Office 2 Lease is for approximately 1,270 square feet of office space, with the Company taking occupancy on October 1, 2024. The Pompano Office 2 Lease has a term of three years, ending on September 30, 2027.

The Company has entered into a lease agreement for approximately 35,000 square feet of floor space in a building located at 144 Ludlow Avenue, Northvale, New Jersey (the “144 Ludlow Ave. Lease”). The 144 Ludlow Ave. Lease began on January 22, 2024, and has a term of five years. The 144 Ludlow Ave. Lease will expire on December 31, 2028. The lease terms also include a Company option to extend the term by two years.

Properties used in our operation are considered suitable for the purposes for which they are used, at the time they are placed into service, and are believed adequate to meet our needs for the reasonably foreseeable future.

Item 2 of the 10-K filed Jun 29, 2026.4

Leadership

Who has led ELITE PHARMACEUTICALS INC /NV/, and when. Pick a name to see everywhere that person has worked.

Board members and other officers (22)

Former names

  • ELITE PHARMACEUTICALS INC /DE/Sep 28, 1998 to Feb 8, 20123

Timeline

  1. Aug 13, 20268-K Results of operations; Regulation FD disclosure46
  2. Aug 11, 20268-K Regulation FD disclosure47
  3. Aug 10, 20268-K Regulation FD disclosure48
  4. Aug 4, 20268-K Regulation FD disclosure49
  5. Jun 29, 20268-K Results of operations; Regulation FD disclosure50
  6. Jun 23, 20268-K Regulation FD disclosure51
  7. Jun 15, 20268-K Regulation FD disclosure52
  8. Jun 1, 20268-K Regulation FD disclosure53
  9. Apr 2, 20268-K Regulation FD disclosure54
  10. Feb 17, 20268-K Results of operations; Regulation FD disclosure55
  11. Feb 11, 20268-K Regulation FD disclosure56
  12. Nov 14, 20258-K Results of operations; Regulation FD disclosure57
  13. Aug 21, 2013New chief executive Nasrat A. Hakim becomes CEO14
  14. Jul 16, 2010New chief executive Jerry Treppel becomes CEO15
  15. Nov 15, 2006New chief executive Bernard Berk becomes CEO16

Calendar

When it reported results

  1. Aug 13, 2026Reported quarterly or annual results46
  2. Jun 29, 2026Reported quarterly or annual results50
  3. Feb 17, 2026Reported quarterly or annual results55
  4. Nov 14, 2025Reported quarterly or annual results57
  5. Aug 14, 2025Reported quarterly or annual results58
  6. Jun 30, 2025Reported quarterly or annual results59
  7. Feb 13, 2025Reported quarterly or annual results60
  8. Nov 14, 2024Reported quarterly or annual results61

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). The full markets calendar

Filings

122 filings to the SEC since October 2021: 6 annual reports, 15 quarterly reports, 66 major events, 23 insider forms, 12 other. The latest 20:

  1. Sep 10, 20264 PRIMARY DOCUMENT EDGAR
  2. Aug 13, 20268-K EDGAR
  3. Aug 13, 202610-Q EDGAR
  4. Aug 11, 20268-K/A EDGAR
  5. Aug 10, 20268-K EDGAR
  6. Aug 4, 20268-K EDGAR
  7. Jun 29, 20268-K EDGAR
  8. Jun 29, 202610-K EDGAR
  9. Jun 23, 20268-K EDGAR
  10. Jun 15, 20268-K EDGAR
  11. Jun 1, 20268-K EDGAR
  12. Apr 14, 2026UPLOAD EDGAR
  13. Apr 2, 20268-K EDGAR
  14. Mar 18, 2026CORRESP EDGAR
  15. Mar 4, 2026UPLOAD EDGAR
  16. Feb 17, 20268-K EDGAR
  17. Feb 17, 202610-Q EDGAR
  18. Feb 11, 20268-K EDGAR
  19. Jan 13, 20264 EDGAR
  20. Nov 14, 20258-K EDGAR

The 122 filings since October 2021 can be filtered by form type and year here when JavaScript is on.

Every filing from the last five years, summarized. The full record is on SEC EDGAR.

Insider trades

7 open-market trades by officers, directors and large owners since October 2021: 2 buys and 5 sales. Grants, option exercises and gifts are left out.

DateWhoTradeSharesPriceValueFiling
Aug 19, 2026Dash Barry HDirectorBuy30,000$0.29$8.7KForm 4
Oct 2, 2025Plassche DouglasEVP OperationsSale800,000$0.62$496.0KForm 4
Aug 22, 2025ELITE PHARMACEUTICALS INC /NV/EVP OperationsSale500,000$0.52$260.0KForm 4
Jul 10, 2025Kirkov KirkoChief Commercial OfficerBuy16,366$0.59$9.7KForm 4
Jul 8, 2025Plassche DouglasEVP OperationsSale200,000$0.58$116.0KForm 4
Oct 24, 2024Plassche DouglasEVP OperationsSale333,932$0.51$170.3KForm 4
Oct 23, 2024Plassche DouglasEVP OperationsSale800,000$0.49$392.0KForm 4

From Forms 4 filed with the SEC.

Held by these funds

The largest holders among investment managers' 13F reports for the quarter ending Jun 30, 2026. Change is in shares since the quarter before.

FundSharesValueShare of the fundChange
Kelleher Financial Advisors1,000$3650.0%+500

13F reports cover disclosed long positions in U.S. stocks only.

SEC filer profile

How ELITE PHARMACEUTICALS INC /NV/ is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.

  • Name on EDGARELITE PHARMACEUTICALS INC /NV/1
  • CIK0001053369
  • Employer ID (EIN)22-35426364
  • Filer statusNon-accelerated filer not an emerging growth company; a smaller reporting company; a shell company4
  • Incorporated inNevada4
  • Fiscal year endsMarch 311
  • Industry code (SIC)2834 Pharmaceutical Preparations1
  • SEC reviewing officeOffice of Life Sciences, Division of Corporation Finance1
  • Business address165 Ludlow Avenue, Northvale, NJ 076471
  • Phone20175026461
  • Shares outstanding1,077,136,442 as of Aug 13, 202613
  • Public float$534.0M as of Sep 30, 20254
  • AuditorForvis Mazars, LLP, Iselin, NJ PCAOB ID 686; no auditor attestation of internal control over financial reporting4
  • On EDGAR sinceJan 30, 19981
  • Filings1,221 in all: 4 (415), 8-K (279), 10-Q (75), 4/A (47), 3 (36), UPLOAD (29), 10-K (25), CORRESP (25)1
    All 52 form types

    SC 13D/A (24), 8-K/A (22), 424B3 (20), DEF 14A (16), CT ORDER (15), DEFA14A (15), SC 13G/A (14), PRE 14A (13), SC 13G (12), 10QSB (10), EFFECT (10), S-3 (10), 10-Q/A (9), SC 13D (9), 5 (7), PRER14A (7), S-8 (7), 10-K/A (6), D (5), S-3/A (5), NT 10-K (4), PREC14A (4), RW (4), S-1 (4), 10KSB (3), 144 (3), 3/A (3), 424B5 (3), REGDEX (3), SB-2/A (3), 424B1 (2), DEFC14A (2), DFAN14A (2), POS AM (2), S-1/A (2), SB-2 (2), 25 (1), 8-A12B (1), 8-A12G (1), ARS (1), DEL AM (1), NT 10-Q (1), PRRN14A (1), S-4 (1)

  • Latest filingsAnnual report (10-K) Jun 29, 2026
    Quarterly report (10-Q) Aug 13, 2026
    Proxy statement (DEF 14A) Apr 29, 2020
    Latest 8-K (8-K) Aug 13, 2026

Securities registered for trading

ClassSymbolExchange
Common Stock, par value $0.001 per shareELTP

From the cover page of the 10-K filed Jun 29, 2026 (Section 12(b) of the Exchange Act).4

Risk factors and legal proceedings

The risks ELITE PHARMACEUTICALS INC /NV/ names in Item 1A of its 10-K filed Jun 29, 2026: 49 risks under these headings, as written.4

  • Business Related Risks
  • The pharmaceutical industry is highly competitive.
  • Natural disasters could cause closures of our facilities and disrupt our operations.
  • Interruptions in operations at our sole facility could have a material adverse effect on our business.
  • We may sell, withdraw or discontinue manufacture of certain products.
  • We may fail to successfully identify, develop and commercialize new products.
  • As our competitors introduce their own generic equivalents of our generic drug products, our revenues and gross margin from such products generally decline, often rapidly.
  • Our operations could be disrupted by failure of our information systems or cyber-attacks.
  • Artificial intelligence based platforms may present new risks and challenges to our business.
  • Delays in generic product development may result in failure to achieve adequate return on investment.
  • Our business is dependent on market acceptance of our products and social and political pressures, including public concern over the abuse of opioids may adversely affect our business.
  • Unstable economic conditions may adversely affect our business.
The other 38 risks
  • We depend on qualified scientific and technical personnel and our ability to attract and retain such personnel.
  • Unsuccessful collaboration or licensing arrangements could limit revenues and product development.
  • A substantial portion of our total revenues is expected to be derived from sales of a limited number of products to a limited number of customers.
  • We depend to a large extent on third-party suppliers and distributors for the raw materials for our products, particularly the chemical compounds comprising the active pharmaceutical ingredients (“API’s”) that we use to manufacture our products, as well as for certain finished goods.
  • We issue price adjustments and other sales allowances to our customers. Although we may establish reserves based on our estimates of these amounts, if estimates are incorrect and the reserves are inadequate, it may result in adjustments to these liabilities that may have a material adverse effect on our financial position and results of operations.
  • Financial and Liquidity Risks
  • We have identified material weaknesses in our internal control over financial reporting which could, if not remediated, adversely affect our ability to report our financial condition, cash flows and results of operations in a timely and fairly stated manner and/or increase the risk of future misstatements, which could have a material adverse effect on our business, financial condition, cash flows and results of operations and could cause the market value of our common shares and/or debt securities to decline.
  • While we currently qualify as a smaller reporting company under SEC regulations, we cannot be certain, if we take advantage of the reduced disclosure requirements applicable to these companies, that we will not make our stock less attractive to investors. Once we lose smaller reporting company status, the costs and demands placed upon our management are expected to increase.
  • Our operating results could fluctuate significantly.
  • Our ability to fund and grow operations is uncertain and we may require additional financing to meet objectives.
  • There is a risk of impairment of significant intangible assets on our balance sheet.
  • GAAP requires estimates, judgments and assumptions which inherently contain uncertainties.
  • Legal and Regulatory Risks
  • The pharmaceutical industry is heavily regulated which creates uncertainty and substantial compliance costs.
  • Disruptions at the FDA, the DEA, the SEC and other government agencies could negatively impact our business.
  • Our business may be adversely affected by legislation or healthcare regulatory reform and initiatives.
  • Use of generics may be limited through legislative, regulatory or efforts of pharmaceutical companies.
  • Our revenues and profits from generic products may decline as a result of changes in regulatory policy.
  • New tariffs, evolving trade policy, and geopolitical factors and military conflicts between the US and other countries may adversely affect our business.
  • The DEA could limit the availability of active ingredients used in many of our products.
  • We received a CRL from the FDA indicating that the SequestOx™ NDA is not ready for approval.
  • Regulatory factors may cause us to be unable to manufacture products or face interruptions in our manufacturing process.
  • Agreements between branded pharmaceutical companies and generic pharmaceutical companies are facing increased government scrutiny in the United States and Internationally.
  • Our reporting and payment obligations under the Medicaid rebate program and other governmental purchasing and rebate programs are complex and may involve subjective decisions. Any determination that we have failed to comply with those obligations could subject us to penalties and sanctions which could have a material adverse effect on our business.
  • Investigations and litigation concerning the calculation of average wholesale prices may adversely affect our business
  • Litigation and Liability Related Risks
  • We may not be able to obtain or maintain adequate insurance coverages.
  • Litigation, product liability claims, product recalls, government investigations and other significant legal proceedings are common in the pharmaceutical industry.
  • We are subject to various fraud and abuse laws which could expose us to criminal sanctions, civil penalties, contractual damages, reputational harm and diminished profits and future earnings.
  • Our products contain controlled substances which may subject us to increased litigation risk and regulation.
  • Mandatory REMS programs could increase the cost, burden and liability associated with the commercialization of certain products.
  • Illegal distribution and third-party sale of counterfeit versions of our products could have a detrimental effect on our reputation and business.
  • Our competitors or other third parties may allege that we are infringing upon their IP, forcing us to expend substantial resources in litigation, the outcome of which is uncertain. Any unfavorable outcome of such litigation, including, without limitation, losses related to “at-risk” product launches, could have a material effect our business, financial position and results of operations.
  • Intellectual Property Related Risks
  • Our ability to protect intellectual property rights and successfully defend against third-party allegations of IP infringement is vital to our business and uncertain.
  • Risks Related to our Common Shares
  • Dilution from issuance of shares upon exercise of warrants and options or the perception that dilution may occur could cause the price per share of common stock to fall.
  • Our common stock is a penny stock, quoted on the OTC bulletin board, with rules in place that could limit trading and liquidity of our shares, increased transaction costs that could adversely affect our price per share.
  • Shareholder activism could negatively affect us.
  • Our stock price has been volatile.
  • Capital raises through sales of securities may cause substantial dilution to existing shareholders.
  • Issuance of shares of common or preferred stock could make achieving a change of control more difficult.
  • We have no plans to pay regular dividends or conduct share purchases.

Legal proceedings

On August 17, 2023, Elite filed a Paragraph IV certification with its ANDA to generic Oxycontin and after Elite got acceptance of the ANDA by the FDA on September 19, 2023, Elite sent the patentee and NDA holder a Notice Letter as required under the Hatch-Waxman Act. On November 14, 2023, a patent infringement suit was filed in the District Court of New Jersey by Purdue Pharma. The parties agreed to a stipulated dismissal of the case and the judge signed the order dismissing the case on June 12, 2026.

Elite’s launch of a generic Oxycontin will depend on approval by the FDA and the outcome of various litigation involving Purdue or the expiry of the patents listed on the Orange Book.

In the ordinary course of business, we may be subject to litigation from time to time. There is no current, pending or, to our knowledge, threatened litigation or administrative action to which we are a party or of which our property is the subject (including litigation or actions involving our officers, directors, affiliates, or other key personnel, or holders of record or beneficially of more than 5% of any class of our voting securities, or any associate of any such party) which in our opinion has, or is expected to have, a material adverse effect upon our business, prospects financial condition or operations. A significant increase in the number of claims or an increase in amounts owing under successful claims could materially adversely affect our business, financial condition, results of operations and cash flows.

The opening of Item 3, Legal Proceedings.4

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