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The following is an excerpt from a 10-K SEC Filing, filed by ROYCE LABORATORIES INC /FL/ on 3/27/1996.

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NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
YEARS ENDED DECEMBER 31, 1995, 1994 AND 1993

NOTE 1. OPERATIONS AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

I. Operations

Royce Laboratories, Inc. (the "Company") is a Florida corporation engaged in developing, manufacturing and marketing generic prescription and non-prescription drugs in solid dosage form (tablets and capsules). The Company sells its products primarily to U.S. based drug wholesalers, generic drug distributors, retail buying groups, managed care organizations and drug chains.

In October 1991, the Company formed a wholly-owned subsidiary, Royce Research Group, Inc. ("RRGI") to engage, through a licensing agreement with the Company, in the development and marketing of five generic prescription drugs (See Note 9).

II. Summary of significant accounting policies

A summary of the significant accounting policies followed by the Company in the preparation of the accompanying financial statements is presented below.

(A) Principles of consolidation

The accompanying consolidated financial statements include the accounts of the Company and its wholly owned subsidiary. All significant intercompany balances and transactions have been eliminated.

(B) Fair value of financial instruments

The financial instruments included in the Company's balance sheets are cash and cash equivalents and long-term debt. These instruments were carried at amounts approximating fair value at December 31, 1995 and 1994. The fair value of long-term debt was estimated based on future cash flows discounted at current interest rates available to the Company for instruments with similar maturities and characteristics.

(C) Concentration of credit risk

The Company is potentially subject to a concentration of credit risk consisting of its accounts receivable, the entire balance of which is due from generic drug distributors, wholesalers, retail buying groups, managed care organizations and drug chains. The Company assesses the financial strength of its customers and does not require collateral. The Company maintains reserves for potential losses from uncollectible accounts.

(D) Cash and cash equivalents

Cash on hand, deposits in banks, and money market funds, and other highly liquid investments with an original maturity of three months or less, are considered cash and cash equivalents.

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

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ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 1. OPERATIONS AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (CONTINUED)

(E) Inventory

Inventory is stated at the lower of cost or market. Cost is determined principally by the first-in, first-out method.

(F) Property and equipment

Property and equipment is stated at cost, less accumulated depreciation and amortization. Depreciation is computed using the straight-line method over the estimated useful lives of the assets. Amortization of leasehold improvements is computed using the straight-line method over the shorter of the lease term or estimated useful lives of the related assets. Expenditures for repairs and maintenance are charged to expense as incurred, while expenditures which extend the useful lives of assets are capitalized.

(G) Income taxes

The Company records income taxes using the liability method. Under this method, deferred tax assets and liabilities are determined based upon differences between financial reporting and tax bases of assets and liabilities and are measured using the enacted income tax rates that will be in effect when the differences are expected to reverse. An allowance is recorded when it is more likely than not that any or all of a deferred tax asset will not be realized. The provision for income taxes includes taxes currently payable plus the net change during the year in deferred tax assets and liabilities recorded by the Company.

(H) Capital

The Company effected a 1-for-3 reverse stock split in December 1993. All share amounts referred to in these financial statements and notes have been adjusted for the stock split.

(I) Revenue recognition

Sales are recorded at the time goods are shipped.

(J) Research and development costs

All research and development costs are expensed as incurred.

(K) Loss per share

Loss per share amounts are computed by dividing net losses by the weighted average number of shares of common stock outstanding during each of the periods. Warrants, options and other common stock equivalents have not been included in the calculation of loss per share because their effect would be antidilutive.

(L) Reclassifications

Beginning in 1995, volume rebates awarded to customers have been recorded in net sales. Prior to 1995, such rebates were recorded in selling expenses. Prior year financial statements have been reclassified to reflect this change. The effect of this reclassification was to decrease net sales and selling, general and administrative expenses by $380,000 and $91,000 for the years ended December 31, 1994 and 1993, respectively.

In addition, certain other amounts in the 1993 and 1994 financial statements have been reclassified to conform to the 1995 presentation.

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-7

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 1. OPERATIONS AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (CONTINUED)

(M) Stock based compensation

In October 1995, the Financial Accounting Standards Board ("FASB") issued Statement of Financial Account Standards No. 123, Accounting For Stock Based Compensation ("SFAS 123"). SFAS 123, the disclosure provisions of which must be implemented for fiscal years beginning subsequent to December 15, 1995, establishes a fair value based method of accounting for stock based compensation plans, the effect of which can either be disclosed or recorded. The Company will adopt the provisions of SFAS 123 in 1996. Upon adoption, the Company intends to retain the intrinsic value method of accounting for stock based compensation, which it currently uses.

(N) Management estimates

The preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. The most significant estimates made by management in the accompanying financial statements relate to accounts receivable allowances. Actual results could differ from those estimates.

NOTE 2. INVENTORIES

Inventories consisted of the following (in thousands):

1995 1994

Raw materials $ 2,439 $ 1,426 Work-in-process 783 284 Finished goods 990 339

$ 4,212 $ 2,049


NOTE 3. PROPERTY AND EQUIPMENT

Property and equipment consisted of the following (in thousands):

DECEMBER 31, ESTIMATED
----------------------------- USEFUL LIVES
1995 1994 (YEARS)

Leasehold improvements $ 529 $ 216 5 - 10 Machinery and equipment 1,948 1,501 3 - 7 Transportation equipment 17 13 3 Furniture and equipment 435 146 3 - 7 2,929 1,876 Less accumulated depreciation
and amortization ( 1,197) ( 896)

$ 1,732 $ 980


THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

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ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 4. LONG-TERM DEBT

Long-term debt consisted of the following (in thousands): DECEMBER 31, ----------------------- 1995 1994 -------- -------- Notes payable to banks, payable in monthly installments, including interest at rates ranging from 9.6% to 10.5% per annum for terms expiring at various dates through March 2000, secured by furniture and equipment. $ 186 $ 58

Capital lease obligations, net of imputed interest of $16, payable in monthly installments including interest at imputed rates ranging from 10.8% to 13.0% per annum for terms expiring at various dates through May 1999, secured by equipment. 85 - ---------- ------------ 271 58 Less current maturities ( 90) ( 25) ---------- ------------

$ 181 $ 33 ========== ============

Annual maturities of long-term debt including capital lease obligations at December 31, 1995 were as follows:

1996 $ 90 1997 81 1998 59 1999 32 2000 9 $ 271


NOTE 5. MAJOR CUSTOMERS

The table below reflects the percentage of total net sales that major customers (i.e., customers who accounted for more than 10% of the Company's total net sales in any year) accounted for:

YEARS ENDED DECEMBER 31,

1995 1994 1993

Customer A 13% 14% 15% Customer B - 10% - Customer C 12% - 12%

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-9

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 6. INCOME TAXES

At December 31, 1995 and 1994, the Company had a deferred tax asset of approximately $6.0 million and $5.4 million, respectively, attributable primarily to net operating loss carryforwards. The Company has established a valuation allowance for 100% of the deferred tax asset due to the uncertainties related to its eventual realizability. The change in the Company's net deferred tax asset and the related valuation allowance in 1995 was due to losses incurred for income tax purposes during the year. The Company has net operating loss carryforwards of approximately $16.0 million for tax purposes which expire between the years 2000 and 2010.

As a result of certain changes in the Company's ownership during 1991, the utilization of net operating loss carryforwards has been limited to approximately $350,000 per year for losses incurred prior to 1991. Future changes in the Company's ownership, if any, may have the effect of further limiting the annual utilization of loss carryforwards.

NOTE 7. OTHER MATTERS

I. Class action settlement

In April 1992, several class action lawsuits were filed against the Company and certain of its officers and directors (the "Defendants"). The complaints alleged that the Defendants had misrepresented the Company's prospects for obtaining final approval from the Food and Drug Administration ("FDA") to manufacture and market Piroxicam. On September 28, 1993, the U.S. District Court approved a settlement of the class action lawsuits. Pursuant to the settlement agreement, the company agreed to (i) pay $850,000 which was funded by the Company's Directors and Officers liability insurance; (ii) issue 250,000 shares of free trading common stock; and (iii) issue five year warrants (See Note 8(III)(E)), to purchase 658,333 shares of free trading common stock at $15.00 per share. All such shares and warrants were distributed in early 1995. In 1993, the Company recorded a charge to earnings of $1,336,000 related to this settlement. Such charge represented the market value of the 250,000 shares on the settlement date.

II. Write off of inventory and receivables

As a result of the Company's withdrawal of its abbreviated new drug applications for Minoxidil, Haloperidol and Piroxicam, the Company wrote off inventory and issued credits to customers in the amounts of $792,000 in 1993.

NOTE 8. CAPITAL STOCK

I. Capital stock - authorized and issued

At December 31, 1995, the Company had authorized 200,000 shares of preferred stock, $.005 par value (the "Preferred Stock"), none of which was issued and outstanding.

In addition to its 12,838,466 common shares issued, the Company had a total of 3,047,143 warrants and options outstanding at December 31, 1995.

II. Stock offerings

A) 1995 Private Placement

During July 1995, the Company completed a $5 million private placement ("1995 Private Placement") of 833,333 units at a price of $6.00 per unit. Each unit consisted of one share of common stock, $.005 par value, and a

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-10

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 8. CAPITAL STOCK (CONTINUED)

twelve month warrant (the "Private Warrants") to purchase one share of common stock at an exercise price of $6.50 per share. The price of the shares was determined in arms-length negotiations between the Company and the placement agent, Gruntal & Co., Incorporated ("Gruntal"). The Company received aggregate net proceeds of approximately $4.4 million from this offering. In addition to fees for serving as the placement agent, Gruntal received three-year warrants (See Note 8(III)(C)) to purchase 83,333 shares of common stock at an exercise price of $6.00 per share.

In August 1995, the Company filed a registration statement relating to the shares of common stock sold in the 1995 Private Placement and the shares of common stock underlying the warrants sold in the private placement. Such registration statement was declared effective under the Securities Act of 1933, as amended, during October 1995. The Company has also agreed to use its best efforts to maintain the effectiveness of the registration statement until July 1997.

On December 12, 1995, the Company reduced the exercise price of the Private Warrants from $6.50 to $6.00 for a 60 day period as an incentive for warrant holders to exercise. Subsequent to December 31, 1995, the Company issued 581,333 shares of its common stock as a result of the exercise of 581,333 Private Warrants. Net proceeds from the exercise of these warrants amounted to approximately $3.4 million.

B) 1994 Private Placement

During September 1994, the Company completed a private placement ("1994 Private Placement") in which the Company sold an aggregate of 2,000,000 shares of its common stock at a price of $2.50 per share. The price of the shares was determined in arms-length negotiations between the Company and Gruntal, which acted as the placement agent of this offering. In addition to fees for serving as the placement agent, Gruntal also received 200,000 warrants (See Note 8(III)(D)). The Company received aggregate net proceeds of approximately $4.1 million from this offering. A registration statement relating to the shares sold in the 1994 Private Placement is effective as of the date of these financial statements.

III. Stock options, warrants and rights

A) Employee and director stock option plans

(1) Description

In 1992, the Company established a stock option plan which provides for the granting at the fair market value of the underlying shares at the date of grant, of incentive options for its employees, officers and directors (the "1992 Plan"). The 1992 Plan provides for the grant of up to 333,333 shares of common stock to officers, directors and other key employees. The 1992 Plan provides for mandatory grants to directors for serving on the Board of Directors, committees of the Board of Directors, as chairman of committees and as Chairman of the Board of Directors. Options granted pursuant to the 1992 Plan expire five years from the date they become vested, which is, in most cases, over a three year period beginning with the grant date. The 1992 Plan is administered by the Compensation Committee of the Board of Directors.

At the Company's annual meeting of shareholders on July 25, 1995, the shareholders approved the Board of Directors' adoption of a new stock option plan (the "1995 Plan"). Under the 1995 Plan, the Board is authorized to issue options to purchase up to 550,000 shares of common stock to officers, directors, and other key employees. The 1995 Plan provides for mandatory grants to directors for serving on the Board of Directors, committees of the Board of Directors, as chairman of committees and as Chairman of the Board of Directors, which mandatory grants of options superceded the options grants provided for in the 1992 Plan. The exercise

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-11

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 8. CAPITAL STOCK (CONTINUED)

price of options granted under the 1995 Plan must equal or exceed the fair market value of the common stock on the date such options are granted. No options issued under the 1995 Plan may be exercised more than ten years from the date of grant. The Compensation Committee of the Board of Directors is responsible for administering the 1995 Plan.

All employee and director options expire at various times between 1996 and 2005.

(2) Employee and director stock option activity in 1995

In 1995, the Board of Directors granted a total of 35,828 stock options under its 1995 Plan to the President and the outside directors for their services on the Board and its committees. These options are exercisable at $8.44 per share and expire in April 2000. During 1995, the Company also granted 110,000 stock options to certain employees of the Company. These options vest generally over three years, are exercisable at prices between $5.91 and $9.00 per share and expire five years from their vesting dates. All of the above options were issued at or above the fair market value of the Company's common stock at the date of grant.

Below is a table summarizing transactions and other relevant data pertaining to employee and director stock options:

NUMBER OF PRICE PER 1992 PLAN OPTIONS SHARE

Options outstanding at December 31, 1992 97,494 $ 9.56 - $25.41 Options granted 113,329 $ 4.50 - $7.69

Options outstanding at December 31, 1993 210,823 $ 4.50 - $25.41

Options granted 85,829 $ 4.63 - $ 5.75

Options outstanding at December 31, 1994 296,652 $ 4.50 - $25.41

Options granted 103,761 $ 5.91 - $9.00 Options exercised ( 9,166) $ 5.75 - $6.63 Options canceled ( 67,080) $19.50 - $25.41

Options outstanding at December 31, 1995 324,167 $ 4.50 - 25.41


1995 PLAN

Options outstanding at December 31, 1994 - - Options granted 42,067 $ 8.44 - $9.00

Options outstanding at December 31, 1995 42,067 $ 8.44 - $9.00


THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-12

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 8. CAPITAL STOCK (CONTINUED)

NON-PLAN STOCK OPTIONS

Options outstanding at December 31, 1992 446,137 $.75 - $25.41

Options granted 9,999 $6.56 Options exercised ( 137,560) $.75

Options outstanding at December 31, 1993 318,576 $.75 - $25.41

Options granted 462,500 $3.00 - $6.75 Options exercised ( 105,665) $.75 Options canceled ( 3,334) $.75

Options outstanding at December 31, 1994 672,077 $.75 - $25.41

Options exercised ( 29,499) $.75 - $6.56

Options outstanding at December 31, 1995 642,578 $.75 - $25.41


At December 31, 1995, 623,809 of the previously described options were vested.

B) 1995 private placement warrants

As part of the Company's 1995 Private Placement, the Company issued 833,333 Private Warrants.

Each Private Warrant entitles the holder to purchase one share of common stock at an exercise price of $6.50 per share. The exercise price is subject to increase or decrease upon the happening of certain corporate events including, but not limited to the payment of any stock dividend, stock split, stock combination or similar transaction. The Private Warrants may be exercised at any time through July 20, 1996, unless such period is extended by the Company.

On December 12, 1995, the Company reduced the exercise price of the Private Warrants from $6.50 to $6.00 for a 60 day period as an incentive for warrant holders to exercise their Private Warrants. Subsequent to December 31, 1995, the Company issued 581,333 shares of its common stock as a result of the exercise of 581,333 Private Warrants. Net proceeds from the exercise of these warrants amounted to approximately $3.4 million.

C) 1995 Gruntal warrant

As part of its compensation for acting as the placement agent in connection with the 1995 Private Placement, Gruntal received the 1995 Gruntal warrant which allows them to purchase 83,333 shares of common stock at an exercise price equal to $6.00 per share, exercisable until July 21, 1998. The holder of the 1995 Gruntal warrant may pay the exercise price in cash or use a cashless exercise. In a cashless exercise, the holder of the 1995 Gruntal warrant has the right at any time to exercise the warrant in whole or in part by surrendering the warrant certificate in exchange for the number of shares of common stock equal to (x) the number of shares as to which the 1995 Gruntal warrant is being exercised multiplied by (y) a fraction, the numerator of which is the market price (as defined in the 1995 Gruntal warrant) of the common stock at the date of exercise less the exercise price and the denominator of which is such market price. The 1995 Gruntal warrant provides for an adjustment of the

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-13

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 8. CAPITAL STOCK (CONTINUED)

exercise price and the number and type of securities issuable upon the exercise thereof upon the occurrence of certain events, including the payment of any stock dividend stock split, stock combination or similar transaction.

D) 1994 Gruntal warrant

As part of its compensation for acting as the placement agent in connection with the 1994 Private Placement, Gruntal received warrants which allow them to purchase 200,000 shares of common stock at an exercise price equal to $3.50 per share, exercisable until August 12, 1999. The holder of the 1994 Gruntal warrant may pay the exercise price in cash or use a cashless exercise. The provisions for a cashless exercise and adjustments to the exercise price are similar to those described above for the 1995 Gruntal warrant.

E) Class action settlement warrants

In accordance with the settlement in 1993 of the class action lawsuit, during the first quarter of 1995, the Company issued warrants to purchase 658,333 shares of common stock (See Note 7(I)). Each of these warrants (the "Series F Warrants") entitles the holder to purchase one share of common stock at an exercise price of $15.00 per share. The Series F Warrants are exercisable through December 1999, unless such period is extended by the Company. The exercise price and the number of shares of common stock to be purchased upon the exercise of each Series F Warrant are subject to increase or decrease upon the happening of certain corporate events, including but not limited to the payment of any stock dividend, stock split, stock combination or similar transactions.

The Series F Warrants may be called at the sole option of the Company upon thirty days prior written notice to the registered holders thereof so long as the common stock trades above $18.00 per share for 20 consecutive trading days ending not more than 10 days prior to the date that the notice of redemption is given. Any such redemption shall be for all outstanding Series F Warrants. If the Company elects to redeem the Series F Warrants, then the Warrant holders shall have the rights to exercise their Series F Warrants until the redemption date, and thereafter, the holder shall only be entitled to receive the redemption price therefor.

F) 1992 public offering warrants

As part of the Company's 1992 public offering, 1,150,000 warrants (the "Public Warrants") were issued. Each Public Warrant entitled the holder to purchase one sixth (1/6) of a share of common stock (six Public Warrants were required to purchase one share of common stock) at an exercise price of $30 per Share. On July 8, 1995, all such warrants expired unexercised.

G) 1992 underwriters warrants

The Company has outstanding underwriters' warrants relating to its 1992 public offering ("the 1992 Underwriters Warrants"). Paradise Valley Securities, Inc. ("PVS"), the managing underwriter of the Company's January 1992 public offering and designees of Chatfield Dean and Co., Inc., one of the underwriters of such offering, own an aggregate of 33,333 1992 Underwriters Warrants to purchase units of the Company's securities at an exercise price of $21.60 per unit. Each unit consists of 2 shares of common stock and a warrant to purchase 1/2 of a share of common stock at an exercise price of $30 per share. The exercise price and the number of shares of common stock and warrants which can be purchased upon the exercise of the 1992 Underwriters' Warrants are subject to increase of decrease upon the happening of certain events, and in the event that the Company issues shares of common stock at less than $9.00 per share. The issuance of the shares of common stock and, if issued, the warrants, will cause a reduction in the exercise price of and an increase in the number of shares of common stock issuable upon the exercise of this warrant. Issuances of securities subsequent to the date of issuance of the 1992

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-14

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 8. CAPITAL STOCK (CONTINUED)

Underwriters Warrants have reduced the exercise price of the units to approximately $17.25 per unit and increased the number of units available for purchase to approximately 40,000 units. The warrants are exercisable through January 9, 1997.

H) 1991 public offering warrants

In August 1993, PVS exercised an "Underwriter's Warrant" issued in connection with the Company's February 1991 public offering. The Underwriter's warrant entitled PVS to purchase 15,300 Units of the Company's securities. Each unit consisted of eight shares of common stock, $.005 par value, and two common stock purchase warrants, at an exercise price of $7.68 per Unit. In connection with the exercise of this Underwriter's Warrant, the Company issued 122,400 shares of its common stock and a warrant to purchase 30,600 shares and received $117,504 from the Underwriter.

On May 2, 1994, PVS exercised their warrant to purchase 30,600 shares of the Company's common stock. The exercise price of the warrant was $3.00 per share, representing an aggregate exercise price of $91,800. PVS paid the Company $45,225, which represents the difference between the aggregate exercise price and a credit of $46,575, which the Company granted to PVS in return for PVS agreeing to waive its right of first refusal contained in the underwriting agreement relating to the Company's 1992 public offering. In connection with this agreement, the Company and PVS executed mutual releases with respect to all matters arising under the 1992 underwriting agreement and with respect to the class action litigation.

I) Customer options

In June 1991, the Company entered into an option agreement with a customer, which agreement was subsequently assigned to the customer's parent. Under the agreement, the customer was granted a five-year option to purchase shares of the Company's common stock at $1.875 per share, upon the satisfaction of certain purchase targets. Options earned are determined as of June 30 of each year based on the previous 12 months' purchases by the customer. As of December 31, 1995, the maximum number of options the customer could earn through the end of this agreement in June 1996 is 106,666 options. If the customer earns options for the contract year ended June 30, 1996 and at that date a spread exists whereby the fair market value per share exceeds the option price (the "Spread"), the Company will record a charge to earnings equal to the Spread times the number of options earned.

In February 1995, the Company entered into an agreement with another customer whereby the customer agreed to engage the Company as its sole supplier of the Company's present and future products for a five year period subject to certain exceptions. In return, the Company granted the customer stock options to purchase up to 50,000 shares of common stock at $6.00 per share, the market price on the date of grant. Such options vest at the rate of 9,000 per year, with 5,000 options vesting upon entering into this agreement. In connection with this agreement, the Company has recorded a charge to earnings of approximately $66,000 in 1995.

J) Anti-takeover right

Certain provisions of the Articles and Bylaws of the Company may be deemed to have an anti-takeover effect and may delay, defer or prevent a tender offer or takeover attempt, including an attempt that might result in a premium being bid over the market price for the shares held by shareholders. Several provisions may not be amended in the Company's Articles and Bylaws without the affirmative vote of the shareholder of 80% of the outstanding shares of common stock.

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-15

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 8. CAPITAL STOCK (CONTINUED)

A supermajority (80%) vote of the shareholders is required to approve certain transactions with an entity of which 10% or more is beneficially owned by a 10% or more shareholder of the company, unless such transaction is approved by a majority of the continuing directors.

The Company has a classified Board of Directors divided into three classes serving staggered terms. At each annual meeting, approximately one-third of the director's terms of office expire for which elections are held. Directors may be removed from office only for cause and only by supermajority vote of the shareholders.

In addition, shareholder action must be effected at a duly called annual or special meeting of the shareholders and may not be effected by written consent. Special meetings are called by the Board of Directors pursuant to a resolution approved by a majority of the entire Board of Directors.

NOTE 9. R&D LIMITED PARTNERSHIP

In 1991, the Company, through its subsidiary RRGI, completed the funding of a research and development limited partnership (the "Partnership"). The Partnership received net proceeds of $1,035,000 from its partners to develop five generic prescription drugs ("Licensed Drugs"). The Partnership's funds were paid, in part, to the Company for its services in developing the Licensed Drugs and to obtain a one-percent royalty interest in the gross revenue derived from the commercial sale of Piroxicam for a three-year period, with the remainder paid to third party vendors used in the development of the products. As remuneration for developing the Licensed Drugs, the Company received $40,000 and $52,000 in 1994 and 1993, respectively, from the Partnership. In return for funding the development of the Licensed Drugs, the Partnership will receive a royalty of 10 percent of the net revenues generated by sales of the Licensed Drugs over a five-year period.

As of March 1, 1996, the Company had received FDA approvals for three of the Licensed Drugs and Piroxicam. Applications are pending for the other two Licensed Drugs. The Company incurred royalty expenses of $69,000 in 1995 related to the sales of the Licensed Drugs and Piroxicam.

NOTE 10. COMMITMENTS AND CONTINGENCIES

I. Operating leases

The Company leases its 25,000 square foot production facility under an operating lease that expires on July 31, 2000 and provides for two five-year renewal options. The Company has also agreed to lease an additional 10,228 square foot space contiguous to its existing space when it becomes available, but no later than November 1996. Pursuant to the lease agreement, the Company also has an option throughout the term of the lease, including renewal periods, to purchase the entire building and an adjacent building at a specified price. Annual rent under the lease is approximately $137,000, subject to annual cost of living increases.

The Company also leases another nearby 40,000 square foot facility which houses its executive offices, warehouse and in the future and, will house its research and development laboratory. The lease is for a 10 1/2 year term, with two five-year renewal options. The lease requires the Company to make annual lease payments of approximately $195,000. The Company also has an option to purchase the leased facility during the first twelve-months of the lease and during the sixth year of the lease at a specified price.

Total rental expense for operating leases was $324,000, $178,000 and $167,000 for 1995, 1994 and 1993, respectively. The terms of the operating leases for the Company's facilities require the Company to maintain minimum insurance coverage and to pay property taxes and repair and maintenance expenses.

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-16

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 10. COMMITMENTS AND CONTINGENCIES (CONTINUED)

At December 31, 1995, future minimum lease payments under all non-cancelable operating leases are as follows (in thousands):

1996 $ 256 1997 260 1998 265 1999 269 2000 216 Thereafter 750

Total minimum lease payments $ 2,016


II. Other commitments

A) Purchase commitments

The Company has entered into a development agreement with a raw material supplier to develop two products and to purchase its raw material requirements for these products from the supplier. So long as the Company files ANDAs, obtains approval of same within a specified time period and thereafter satisfies certain purchase requirements, the supplier has agreed that the Company shall be its only customer for this raw material in the United States, Canada and Mexico. The Company currently has ANDAs pending for both products.

B) Product license agreement

In August 1993, the Company entered into a perpetual license agreement with the formulator of a drug whereby the Company has agreed to pay the formulator a sliding royalty with a maximum of 10 percent of net sales of this product for a ten-year period. In 1994, the Company paid the formulator certain fees ($70,000 in cash) when the Company received an acceptable bioequivalency study for this drug and charged such fees to expense. In 1995, the Company issued the formulator 10,695 shares in unregistered common stock upon the filing of an ANDA for this drug and accordingly charged $24,000 to expense. In 1995, the royalty expense incurred for this product was $38,000.

C) Foreign distribution agreements

On July 31, 1994 the Company entered into a license agreement with an Australian pharmaceutical manufacturer with respect to the licensing of one or more products developed by the Company. The license permits the Australian manufacturer to develop, manufacture and market the licensed products in the Pacific Rim markets, including Australia, New Zealand, Japan, Taiwan and Hong Kong (the "Territory").

Although the Company and the Australian manufacturer have agreed on the first product to be licensed under the agreement, there can be no assurance that any other products will be licensed under such agreement. The Company is not obligated under such agreement to license any products to the Australian manufacturer other than the first product, and the Australian manufacturer is not obligated to accept and license any additional product from the Company. Under the agreement, the Company will receive a royalty from the Australian manufacturer with respect to any sales of the licensed products by such manufacturer in the Territory.

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-17

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 10. COMMITMENTS AND CONTINGENCIES (CONTINUED)

In November 1994, the Company entered into a license agreement with a Canadian pharmaceutical company. Pursuant to the agreement, the Canadian company licensed the right to manufacture or purchase from the company at normal selling prices and distribute eight of the Company's products under its private label. Under the agreement, the Company will receive a royalty on the Canadian company's sales of the licensed products in Canada.

III. Employment Contracts

In 1994, the Company entered into employment contracts with certain officers, the most significant of which is with the Company's President. The President's contract provides for an annual base salary, plus cost of living increases, plus a bonus equal to three percent of pre-tax income, the total not to exceed three times the President's base salary. Additionally, the President was granted options to purchase up to 250,000 shares of common stock at a price of $6.75 per share. Such options become exercisable at the rate of 50,000 each January 1st, beginning January 1, 1994. The agreement and these options expire December 31, 1998. The President has agreed not to compete with the Company for a period of eighteen months after termination of his employment.

Each contract with the Company's other officers provides for a minimum base salary, bonuses and stock options, which generally vest over a three-year period. These contracts expire at various dates between 1995 and 1997.

IV. Contingencies

A) Litigation

In February 1993, the Securities and Exchange Commission initiated a formal investigation into possible violations of the federal securities laws by the Company and certain of its officers and directors. The SEC's examination is focusing on the Company's public disclosure during the period between July 1991 and April 1992 regarding the status of the Company's ANDAs for Piroxicam and Minoxidil and on sales of securities during this period by certain persons, including Company executive officers and/or directors. The Company believes that the SEC's investigation is ongoing. While no assurances can be given as to the outcome of the SEC's investigation, the Company does not believe such outcome will have a material adverse effect on the Company's financial condition or results of operations.

On January 12, 1994, the Company was served with a suit brought by one of its shareholders who opted out of the Company's settlement of the class action litigation settled during 1993. The suit, DINESH SHAH V. ROYCE LABORATORIES, INC. AND CHATFIELD DEAN & CO., INC., 94 CIV 0061 (S.D. N.Y.) which has also been brought against one of the underwriters of the Company's January 1992 public offering, alleges that the Company's Janu ary 9, 1992 prospectus was false and misleading. The suit seeks rescissory damages for violations of
Section 11 of the Securities Act of 1933 in the amount of approximately $40,000 plus interest. The Company is vigorously defending this suit and believes it has a meritorious defense. No assurances can be given as to the outcome of this matter.

On August 4, 1995, the Company was sued by Bristol-Myers Squibb Company, Inc. and E.R. Squibb & Sons, Inc. (collectively, "Bristol-Myers") in the Southern District of Florida with respect to Captopril (Case No. 95- 1682-CIV-Davis).

THE ACCOMPANYING NOTES ARE AN
INTEGRAL PART OF THESE FINANCIAL STATEMENTS.

F-18

ROYCE LABORATORIES, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)

NOTE 10. COMMITMENTS AND CONTINGENCIES (CONTINUED)

In March 1995, the Company received a tentative approval of its ANDA for Captopril, the Company's generic equivalent to Bristol-Myers' anti-hypertensive drug Capoten(R). Under the General Agreement on Tariffs anD Trade ("GATT") treaty implementing legislation, patent protection for Capoten(R) was extended from August 8, 1995 until February 13, 1996. The Company asserted, in a certification (the "Certification") filed with the FDA, that under GATT, the Company should have the right to market Captopril after August 8, 1995, subject to the Company's possible obligation to pay "equitable remuneration" to Bristol-Myers on the Company's sales of Captopril during the period between August 8, 1995 and February 13, 1996 (the "Delta Period"). Bristol-Myers suit against the Company was filed based upon the Company's filing of the Certification.

On August 25, 1995, the District Court determined that under the GATT treaty, the Company's manufacture, use or sale of Captopril during the Delta Period would not infringe upon Bristol-Myers' patent for Capoten(R). Based upon this determination, the District Court granted the Company's Emergency Motion to set aside the statutory injunction which arises automatically upon the filing of an infringement action. The District Court further dismissed Bristol-Myers' complaint for patent infringement. However, the District Court denied the Company's request that the District Court order an immediate effective date of the Company's ANDA for Captopril.

Bristol-Myers appealed the decision of the District Court and on November 1, 1995, the United States Court of Appeals for the Federal Circuit (the "Circuit Court") reversed and remanded, with instructions, the decision of the District Court. The Circuit Court, in its ruling, determined that as a matter of law, the safe harbor provisions of GATT do not permit the Company to make, use or sell Captopril prior to February 13, 1996. The Circuit Court further concluded that as a result of its finding, the statutory bar against FDA approval of the Company's ANDA for Captopril prior to February 13, 1996 remained in effect. The Company appealed the Circuit Court's decision to the U.S. Supreme Court however, the Supreme Court did not grant certiorari and the matter has now been remanded to the District Court.

While there can be no assurance, the Company does not believe that this litigation will have a material adverse impact on its financial position or results of operations.

In the ordinary course of business, the Company is at times involved in other legal actions and proceedings. Presently, there are no such actions which are expected to have a significant effect on the Company's operations.

THE ACCOMPANYING NOTES ARE AN