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TAX COURT COMMITTEE ON OPINIONS TAX COURT OF NEW JERSEY DOCKET NO. 000120-1999 CHIRON CORPORATION, : In the New Jersey Tax Court Reports Plaintiff : v. : DIRECTOR, DIVISION OF TAXATION, : Defendant. : Decided: November 19, 2004 Kenneth J. Norcross for plaintiff (Drinker, Biddle & Reath, attorneys). Marlene G. Brown, for defendant (Peter C. Harvey, Attorney General of New Jersey, attorney). KUSKIN, J.T.C. Plaintiff Chiron Corporation, a Delaware corporation with its corporate headquarters in California, has appealed assessments of corporation business tax (CBT) for tax years 1992, 1993, and 1994 imposed by the defendant Director of the New Jersey, Division of Taxation (Director) under the New Jersey Corporation Business Tax Act, N.J.S.A. 54:10A-1 to -41. Specifically, the appeal challenges the Directors computation of plaintiffs sales fraction (also called the receipts fraction), pursuant to N.J.S.A. 54:10A-6, with respect to revenue plaintiff received from its joint business with Ortho Diagnostic Systems, Inc. (ODS) located in New Jersey. * The sales fraction, along with property and payroll fractions, is used to allocate See footnote 1 a portion of a corporations income to New Jersey when the corporation maintains a regular place of business outside of this State. See Mayer & Schweitzer, Inc. v. Director, Div. of Taxation, 20 N.J. Tax 217, 223-25 (Tax 2002) (describing in detail the functioning and components of the apportionment formula set forth in N.J.S.A. 54:10A-6). The numerator of the sales fraction includes, among other items, the taxpayers receipts from sales of personal property shipped into New Jersey, receipts from services performed in New Jersey, and royalties from the use of patents and copyrights in New Jersey. Plaintiff asserts that: the revenue it received from the joint business, as consideration for a license of certain patents and know-how and sale of certain biological products, should be excluded from the numerator of plaintiffs sales fraction because the joint business did not constitute a separate entity and, therefore, plaintiff, in effect, paid the revenue to itself; even if the joint business constituted a separate entity, the relationship between plaintiff and the entity qualified for the flow through method of calculating plaintiffs allocation factor, and thus its sales fraction, under guidelines issued by the Director; and royalty revenues received by plaintiff in connection with a sublicensing by the joint business to Abbott Laboratories (Abbott) of patents and know-how for one of plaintiffs products should be excluded from the numerator of the fraction because the patents and know-how were not used in New Jersey. Both plaintiff and the Director have moved for summary judgment. For the reasons set forth below, I hold that: the joint business constituted a separate Partnership entity domiciled in New Jersey; all revenue received by plaintiff in connection with its sales to the joint business should be included in the numerator of the sales fraction; for purposes of calculating plaintiffs allocation factor and included sales fraction, the flow through method does not apply; and plaintiffs share of royalty revenue from Abbott was derived from Illinois and is not includable in the numerator of the sales fraction. Consequently, I grant defendants motion for summary judgment in part and grant plaintiffs motion in part. Facts The following factual background has either been stipulated by the parties or is not in dispute. Plaintiff is a Delaware corporation with its corporate headquarters in California. It is engaged primarily in the business of manufacturing antigens and antibodies usable for detecting the hepatitis C virus (HCV) and the human immunodeficiency virus (HIV) and manufacturing other biological agents usable to detect human diseases. Because plaintiff lacked adequate capabilities to manufacture, market, and sell test kits using its technology, on October 3, 1986, it entered into a license, research, and supply agreement (the 1986 Agreement) with ODS, which had the experience and capabilities that plaintiff lacked in the development, testing, manufacturing, and marketing of diagnostic products. This agreement provides background to a second agreement dated August 17, 1989 (the 1989 Agreement), which terminated and superseded the 1986 Agreement and was in effect during the years under appeal. Under the 1986 Agreement, plaintiff agreed to conduct a research program for the development of antigens and antibodies to be used for diagnostic testing. Each party agreed to contribute certain funds to finance the research program, and ODS agreed to perform clinical and pre-clinical trials with respect to any antigens and antibodies developed by plaintiff. Plaintiff granted ODS an exclusive worldwide license to plaintiffs inventions, discoveries, trade secrets, information, experience, data, formulas, procedures, and results developed during the research program and any patents which plaintiff might obtain in connection with such research. ODS granted to plaintiff a worldwide non-exclusive royalty free license for inventions, discoveries, trade secrets, information, experience, data, formulas, procedures, and results and improvements thereon relating to ODSs use of antigens and antibodies and development of test kits using the antigens and antibodies. Plaintiff further agreed to supply to ODS all of ODSs requirements of antigens and antibodies. ODS agreed to purchase its requirements from plaintiff, and pay plaintiff for eighty percent of ODSs forecasted requirements even if it did not purchase that amount. The 1986 Agreement established a supervisory board consisting of three senior executives from each of plaintiff and ODS, the function of which included overseeing performance by the parties of their respective obligations under the Agreement, reviewing and analyzing research developments, encouraging and facilitating cooperation between the parties, and suggesting new areas of research and development for the antigens and antibodies provided by plaintiff and for test kits manufactured by ODS, including possible acquisition of third-party technology. Prior to August 17, 1989, plaintiff and ODS became aware that Abbott, an Illinois corporation, was interested in receiving a license to use some of the same technology and know-how that plaintiff had licensed to ODS. In order to facilitate an agreement with Abbott, plaintiff and ODS entered into the 1989 Agreement which had an initial term of fifty years with automatic five-year renewals thereafter. The Agreement recites that its purpose is to restructure and expand the scope of the 1986 Agreement and provide for the sublicensing of certain rights to Abbott. Under the 1989 Agreement, plaintiff was primarily responsible for research and for manufacturing antigens and antibodies for use in detecting HCV and HIV, and ODS was primarily responsible for development, marketing, and sales of Products, defined as immunoassay, immunoassay kits, and immunoassay test configurations using the antigens and antibodies provided by plaintiff. As in the 1986 Agreement, plaintiff agreed to supply ODSs requirements for antigens and antibodies, and ODS agreed to purchase its entire requirements from plaintiff. The minimum payment obligation imposed on ODS in the 1986 Agreement was eliminated from the 1989 Agreement, and the 1989 Agreement protected plaintiff only if ODS had quarterly requirements greater than 130% of its initially forecasted requirements. All deliveries of antigens and antibodies were expressly defined as being F.O.B. at plaintiffs plant in California, with title and risk of loss to pass to ODS upon acceptance of delivery at plaintiffs facility. Although the 1989 Agreement obligated plaintiff to use its best efforts to supply ODS with its requirements for antibodies and antigens, ODS had no express obligation to use the antigens and antibodies to manufacture Products or to sell or market any minimum quantity of Products. ODS had the right to reduce or cease entirely the commercial sale of any Products using plaintiffs antigens and antibodies for detection of HCV. Plaintiff had the right to transform the agreement into a non-exclusive license with respect to all non-HCV products and all antigens and antibodies other than HCV antigens and antibodies if ODS failed to achieve and maintain minimum sales of $5,000,000 per year of non-HCV products. The management structure for the joint business under the 1989 Agreement consisted of a supervisory board as under the 1986 Agreement. The board retained the responsibilities set forth in the 1986 Agreement, but the 1989 Agreement expanded the boards power and authority to include consideration and approval of an annual strategic plan and an annual budget for the business. The board continued to consist of three senior executives from each of plaintiff and ODS. If the representatives of the two entities could not agree on a strategic plan or budget, then the 1989 Agreement authorized ODS in its sole discretion to determine the strategic plan and the budget for the following year as well as the allocation of operating expenses to specific budget categories. ODS also had the sole discretion to assign responsibilities to the parties for the performance of specific functions contemplated by the strategic plan, except that plaintiff would be responsible for research and manufacturing antigens and antibodies. If, however, the sublicensing revenue from Abbott did not exceed specified amounts, then the strategic plan and budget for the next year would be determined by a neutral third party. The authority of the supervisory board was also limited by the 1989 agreement to the extent that the operating expenses allocated to plaintiff for research and development could not exceed 30% of the total expense budget and the expenses allocated to ODS could not exceed 70% of the total expense budget for the business enterprise. The 1989 Agreement provided that, the parties shall in good faith endeavor to spend up to the limits provided for [in an approved budget]. Plaintiff granted to ODS an exclusive worldwide license, without the right to sublicense (with certain specific exceptions) of plaintiffs know-how and any of plaintiffs patents to make, have made, use and sell Products within the Field of Use, and, to the degree necessary, any further license necessary to make the warranties made by Chiron and ODS in the Abbott Immuno Diagnostics Agreement true and complete in all respects. The definition of Products in the 1989 Agreement was the same as in the 1986 Agreement, that is, immunoassays, immunoassay kits, or test configurations which contained antigens or antibodies provided by plaintiff. The definition of Field of Use was the use of any immunoassay for the direct or indirect detection of hepatitis viruses or retroviruses in humans or human samples. In the 1989 Agreement ODS granted to plaintiff a worldwide non-exclusive, royalty-free license, without the right to sublicense for the use of ODSs know-how and patents to be used by plaintiff in its research, manufacturing and other obligations under the Agreement and under the agreement with Abbott. ODS was granted permission to sublicense to Abbott under the license ODS received from plaintiff. Plaintiff and ODS shared equally in the profits generated by the joint business from the sale of blood testing kits, after reimbursement to them of their respective expenses as authorized in the budget, and they shared equally in royalty payments from Abbott. If the business suffered a loss, each party shared equally in the amount of the loss. The parties agreed to cooperate in obtaining an agreement by Abbott to pay plaintiff directly a portion of the royalty payments to be made by Abbott and to reimburse plaintiff directly for certain expenses. The Agreement also provided that, if it terminated, neither the sublicense granted to Abbott nor Abbotts right to use the technology covered by the sublicense would terminate. The 1989 Agreement did not provide for the preparation of separate financial books and records for the joint business, but each party was obligated to provide the other with a written report at the end of each calendar quarter setting forth, in the case of plaintiff, its expenses for the quarter, and, in the case of ODS, its revenues received and expenses for the quarter. The 1989 Agreement provided that the parties owned jointly any patent or know-how invented by them jointly and that each would attempt to obtain a license for the use of any competitive technology and the right to sublicense that competitive technology to Abbott. Advertising with respect to the subject matter of the Agreement had to contain the names of both plaintiff and ODS. The 1989 Agreement was amended on December 22, 1989 so as to permit plaintiff and ODS to acquire tangible assets and intangibles from DuPont. Each party was granted the right to use the purchased assets to the extent necessary or appropriate to carry out the business contemplated by the Agreement. Under the agreement with DuPont, plaintiff and ODS together received a paid-up exclusive license to use certain DuPont patents, customer lists, product information, and research and development information. A second amendment to the 1989 Agreement, dated October 12, 1993, eliminated ODSs obligation to purchase its requirements of antigens and antibodies from plaintiff. Under the amendment, ODS had the right to elect to obtain those materials from plaintiff, and, to the extent ODS so elected, plaintiff was obligated to supply the materials. Simultaneously with the entry into the 1989 Agreement, plaintiff and ODS entered into a License and Supply Agreement with Abbott (the Abbott Agreement). Under this document, ODS, as holder of a license from plaintiff, sublicensed to Abbott plaintiffs technology as to HCV and granted Abbott a worldwide, non-exclusive license to use the antigens and antibodies provided by plaintiff for research purposes and for purposes of making and selling immunoassays, immunoassay kits, and immunoassay test configurations for the detection of HCV. Plaintiff agreed to supply, and Abbott agreed to purchase from plaintiff, all of Abbotts requirements for antigens and antibodies. The Abbott Agreement further provided that, if the 1989 Agreement terminated, Abbotts rights under its sublicense would not be terminated. Abbott granted to plaintiff and ODS a worldwide, non-exclusive license to use Abbotts know-how and technology and to make, use, and sell immunoassays and kits using that know-how and technology. Abbott agreed to pay ODS a specific price for each assay that could be performed using an immunoassay, immunoassay kit, or immunoassay test configuration manufactured by Abbott using the sublicensed technology. In addition, Abbott agreed to pay to ODS, 110% of plaintiffs manufacturing cost for antigens and antibodies supplied to Abbott, except that Abbott agreed to pay directly to plaintiff an amount based on $250 per milligram of antigens and antibodies delivered, plus 20% of plaintiffs manufacturing cost. All amounts paid directly to plaintiff were to be credited against the amounts otherwise payable to ODS. The 1989 Agreement provided that any amounts paid directly to plaintiff by Abbott under the Abbott Agreement could be offset against plaintiffs share of profits from the joint business. In November 1993, plaintiff and ODS entered into an agreement with Pasteur Sanofi Diagnostics (PSD), a French company, granting it a limited, non-exclusive license under patents of plaintiff or ODS or as to which either of them had a license, for purposes of having PSD make, import, use and sell HCV immunoassay products. The Background section of the agreement describes the relationship between plaintiff and ODS as follows: Pursuant to an Agreement dated August 17, 1989 between Ortho and Chiron (the Ortho/Chiron Agreement) Chiron and Ortho together are engaged in a long-term collaborative effort for the joint research, development and commercialization of certain immunoassays, including but not limited to assays of the type licensed under this Agreement. Chiron and Ortho are entering into this Agreement as part of such collaborative effort.
On September 19, 1984, plaintiff and Merck & Co., Inc., entered into an
agreement for which plaintiff licensed to Merck certain patentable and unpatentable inventions and
technologies developed by plaintiff. Merck agreed to pay plaintiff royalties in specified amounts
for the use of the license. Merck was a New Jersey corporation with
its corporate offices in New Jersey, and, for purposes of determining the numerator
of plaintiffs sales fraction, the Director determined that the royalty payments from Merck
should be included. The Director also determined that royalties paid to plaintiff by
Ethicon, a New Jersey corporation with its offices in New Jersey, for licensing
of plaintiffs technology were to be included in the numerator of plaintiffs sales
fraction. Partnership or Joint Venture Under N.J.S.A. 54:10A-6, the sales fraction is defined in pertinent part as follows:
The sales fraction is the receipts of the taxpayer, computed on the cash
or accrual basis according to the method of accounting used in the computation
of its net income for federal tax purposes, arising during such period from
. . .
Plaintiff does not dispute that its sales of antigens and antibodies to ODS
are included under item (2) of the definition. Plaintiff contends, however, that its
relationship with ODS was a joint venture, and that, consequently, one-half of its
sales of antibodies and antigens to the joint venture constituted sales to itself.
Plaintiffs position is summarized in its brief as follows:
Plaintiff asserts that the following announcement published in State Tax News supports its
position:
[N.J. Div. of Taxation, 25 State Tax News, Spring 1996, at 4 (citation
omitted).]
Plaintiff characterizes its relationship with ODS as a joint venture on the following
bases:
[Walter v. Holiday Inns, Inc.,
784 F. Supp. 1159, 1167 n.10 (D.N.J. 1992)
affd,
985 F.2d 1232 (3d Cir. 1993).]
See also, Rodin Properties-Shore Mall, N.V. v. Cushman & Wakefield of Pennsylvania, Inc.,
49 F. Supp.2d 728, 736 (D.N.J. 1999) (defining the elements of a
joint venture as virtually identical to those of a partnership). In Wittner v.
Metzger,
72 N.J. Super. 438 (App. Div. 1962), the court quoted the following
from Cooperstein v. Shapiro,
122 N.J. Eq. 238, 241 (E. & A. 1937):
[Wittner v. Metzger, supra, 72 N.J. Super. at 444.] The Flow Through Method Having determined that the joint business constitutes a partnership, and thus a separate entity for CBT purposes, I next must address plaintiffs argument that it was so integrated with the entity that plaintiffs income allocation factor under N.J.S.A. 54:10-6, and therefore the sales fraction component of the allocation factor, should be calculated using the flow through method (denominated flow through accounting apportionment in N.J.A.C. 18:7-7.6(g)). See footnote 2 If the flow through method is not applicable, the separate entity method (denominated separate accounting apportionment in N.J.A.C. 18:7-7.6(g)) would be used to calculate the allocation factor, and thus the sales fraction, for a corporation, such as plaintiff, owning a partnership interest. N.J.A.C. 18:7-7.6(g)(1) and Example I. See also New Jersey Division of Taxation, Technical Bulletin-3, issued June 21, 1991 and expiring June 30, 1992 (discussed below). Under the separate entity method, the corporations allocation factor, and thus its sales fraction, is calculated by determining a separate allocation factor (using a separate sales fraction) for the partnership and a separate allocation factor (using a separate sales fraction) for the corporation. The partnerships sales fraction has, as its numerator, the partnerships New Jersey receipts (as defined in N.J.S.A. 54:10A-6(B)) and, as its denominator, the partnerships total receipts. The corporations sales fraction has, as its numerator, the corporations New Jersey receipts and, as its denominator, the corporations total receipts, with receipts attributable to the partnership excluded from both the numerator and denominator. Separate property and payroll fractions for the partnership and for the corporation also are calculated using a similar methodology. The allocation factor (representing, for the years under appeal, an average of the sales, property, and payroll fractions See footnote 3 ) for the partnership then is multiplied times the corporations distributive share of partnership income, and the allocation factor for the corporation is multiplied times the corporations income exclusive of its distributive share of partnership income. The total of the two amounts so determined constitutes entire net income (defined in N.J.S.A. 54:10A-4) used to calculate CBT liability under N.J.S.A. 54:10A-5 (setting forth how the tax is to be computed). Under the flow through method, a single allocation factor is calculated for the partnership and the corporation. The sales, property, and payroll fractions comprising the allocation factor have, as their respective numerators, the corporations New Jersey receipts, New Jersey property, and New Jersey payroll (including the corporations share of the partnerships New Jersey receipts, property, and payroll, respectively). The fractions have, as their respective denominators, the corporations total receipts, property, and payroll (including the corporations share of the partnerships total receipts, property and payroll, respectively). The single allocation factor is then multiplied times the corporations entire net income, including its distributive share of partnership income, and the amount so determined constitutes entire net income used to calculate the corporations CBT liability. N.J.A.C. 18:7-7.6(g)(2) and Example III. See also Technical Bulletin-3, supra. Under the facts before me, I infer that, under the separate entity method, the allocation factor by which the Partnerships income would be multiplied to determine plaintiffs share of Partnership income taxable in New Jersey would be larger than the allocation factor by which plaintiffs income (including income from the Partnership) would be multiplied under the flow through method. That is, the denominator of the flow through method allocation factor would be larger in relation to the numerator than would be the case for the separate entity method allocation factor calculated for the Partnership alone. I further infer that this would occur because the sales fraction included in plaintiffs flow through method allocation factor would be reduced by plaintiffs substantial non-Partnership revenues derived from business outside New Jersey, and because plaintiffs property and payroll fractions would be significantly smaller than its sales fraction. Consequently, under the flow through method, the amount of plaintiffs distributive share of Partnership income allocated to New Jersey would be lower than the amount allocated under the separate entity method. Plaintiffs contention that the flow through method should be used is based on Technical Bulletin No. 3, issued by the Division of Taxation on June 21, 1991, and published in State Tax News. N.J. Div. of Taxation, 20 State Tax News, May/June 1991 at 49-51. The Bulletin states that the Division generally treats a partnership as a separate entity from its partners and that, consistent with this theory, the only item that a corporate partner may reflect in its New Jersey allocation factor is the partners distributive share of partnership income. The Bulletin then sets forth circumstances under which the flow through method may apply: In a particular instance a partnership may be so integrated with a corporate taxpayers business and/or the entity theory may lead to such a distortion or elimination of the entire net income of the corporate partner that either the taxpayer or the Division may look through the entity to the partnerships nexus and/or apportionment factors under an aggregate approach.
In such a situation, nexus may exist by virtue of the partnerships activities
in New Jersey, and the receipts, property and payroll of the partnership may
be included in a corporate taxpayers fractions of its allocation factor.
Facts that either singly or in combination may suggest that a flow-through approach
may be appropriate include:
In 1997, after the last year under appeal in this matter, the Director
incorporated the contents of the Technical Bulletin into his regulations under the CBT
Act. N.J.A.C. 18:7-7.6(g).
29 N.J. Reg. 1686(a) and 4327(a) (1997).
See footnote 4
The Abbott Royalties The remaining issue presented by plaintiffs appeal is whether royalty revenues plaintiff received from the Abbott sublicense are includable in the numerator of plaintiffs sales fraction. Plaintiff does not dispute that royalties from a sublicense can be taxed in New Jersey. See N.J.A.C. 18:7-8.11(a)(2) (Receipts from royalties include all amounts received by the taxpayer for the use of patents or copyrights, whether or not such patents or copyrights were originally issued to or are owned by the taxpayer.). Plaintiff contends that, under the express language of N.J.S.A. 54:10A-6(B)(5) (requiring inclusion in the sales fraction of royalties from the use of patents . . . within the State), royalty revenues are allocable to New Jersey only if a patent is used in this State for production of goods. Plaintiff asserts that Abbott used the patents and know-how sublicensed to it for production of blood testing kits in Illinois, and, therefore, the royalties that Abbott paid do not constitute New Jersey revenue. In support of its position, plaintiff cites the Directors treatment, as New Jersey revenue, of royalties payable to plaintiff by Merck & Co. and Ethicon, both located in New Jersey. Plaintiff describes Abbotts payments to ODS in New Jersey as reflecting administrative convenience which should not be the basis for treating plaintiffs share of the Abbott royalties as New Jersey revenue. Plaintiff describes Abbotts direct payments to it, pursuant to the Abbott Agreement, as confirming the use of plaintiffs patents and technology in Illinois. The Director does not dispute that Abbott used, in Illinois, the patents and know-how covered by the sublicense but contends that the Partnerships use, in New Jersey, of the license from plaintiff for the manufacture of blood testing kits and in connection with the agreement with Abbott is sufficient to characterize the Abbott royalties as New Jersey revenue. The Director asserts that the sublicense to Abbott was merely an aspect of the use in New Jersey of plaintiffs patents and know-how, with the other aspect of the use being the manufacture and marketing of blood testing kits. I conclude that, because N.J.S.A. 54:10A-6(B)(5) designates royalties as a separate and independent category of receipts in calculating the sales fraction, I should analyze the Abbott royalties revenue separately from, and independently of, revenue generated by any other use of plaintiffs patents and know-how. For the reasons set forth below, I further conclude that the Abbott royalties revenue is generated by Abbotts use, in Illinois, of plaintiffs patents and know-how under the sublicense from the Partnership. Consequently, the royalty revenue is not includible in the numerator of plaintiffs sales fraction. No reported case in New Jersey has interpreted what constitutes a use of a patent under N.J.S.A. 54:10A-6(B)(5). The Directors regulation states that a patent is used in New Jersey to the extent that activities thereunder are carried on in New Jersey. N.J.A.C. 18:7-8.11(a)(3). Plaintiffs contends that the activities to which the statute and regulation refer must involve production of goods using the licensed patents and know-how. This contention is consistent with the following definition of use of a patent in the Uniform Division of Income for Tax Purposes Act (UDITPA) See footnote 5 for purposes of determining whether income should be allocated to a state: A patent is utilized in a state to the extent that it is employed in production, fabrication, manufacturing, or other processing in the state or to the extent that a patented product, is produced in the state. UDITPA § 8(b), 7 U.L.A. 167 (2002). See also Jerome R. Hellerstein and Walter Hellerstein, State Taxation, supra, at ¶ 9.08 (discussing UDITPA). The royalty revenue under Abbotts sublicense from the Partnership was generated, for the years under appeal, in Illinois by Abbotts use of plaintiffs patents and know-how to manufacture blood testing kits. The Partnerships role in the arrangement with Abbott was a passive one. The Partnership, through ODS, granted the sublicense, and, through ODS, received from Abbott and distributed to plaintiff and ODS the royalty revenue from Abbott (other than the amounts Abbott paid directly to plaintiff). These activities do not constitute a use of plaintiffs patents and know-how in New Jersey within the meaning of N.J.S.A. 54:10A-6(B)(5) or N.J.A.C. 18:7-8.11(a)(3). Our Supreme Court has held that, in deciding whether income is taxable in New Jersey, a court should determine the real source of the income. Avco Financial Services Consumer Discount Co. One, Inc. v. Director, Div. of Taxation, 100 N.J. 27, 36 (1985), Cf. Stryker Corp. v. Director, Div. of Taxation, 168 N.J. 138, 162 (2001) (interpreting N.J.S.A. 54:10A-6(B)(6) to require inclusion in the numerator of the sales fraction of revenue attributable to sales in New Jersey to a New Jersey purchaser even though the New Jersey seller shipped the products directly to out-of-state customers of the purchaser). The real source of plaintiffs income with respect to the Abbott sublicense is Abbotts manufacturing and marketing operations in Illinois. The royalties Abbott pays, therefore, are not New Jersey income and may be excluded from the numerator of plaintiffs sales fraction. Based on the preceding analysis and discussion, defendants motion for summary judgment is granted as to the partnership status of the joint business between plaintiff and ODS and as to the non-applicability of the flow through method, but the motion is denied as to the inclusion of the Abbott royalty revenue in the numerator of plaintiffs sales fraction. Plaintiffs motion for summary judgment is denied as to the partnership and flow through issues, but is granted as to the non-inclusion of the Abbott royalty revenue in the numerator of plaintiffs sales fraction.
Footnote: 1 The applicable New Jersey statutes use the terms allocate and allocation. N.J.S.A. 54:10A-6 and -6.1a. In his regulations, the Director has used allocation, N.J.A.C. 18:7-7.1, -7.3, -7.4 and -7.5, and apportionment. N.J.A.C. 18:7-7.6. The distinction between apportionment and allocation is significant under some circumstances. See Jerome R. Hellerstein and Walter Hellerstein, State Taxation § 9.01 n.2 (3d ed. 2001-2003) where the authors state as follows: The terms allocation and apportionment are sometimes used interchangeably in state statutes and decisions in referring to the formulary method of dividing income or other tax measures. Most state statutes, however, . . . distinguish the two terms. In these states, allocation refers to the attribution of a particular type of income to a designated state, whereas apportionment refers to the division of the tax base by formula. In New Jersey allocation and apportionment are used interchangeably. In this opinion, I use the allocation terminology of N.J.S.A. 54:10A-6 and -6a. Footnote: 2 The allocation factor, the function of which is to allocate corporate income to New Jersey under the CBT Act, consists of a sales fraction, property fraction, and payroll fraction. N.J.S.A. 54:10A-6. In this matter, only the sales fraction is in issue. No proofs were presented as to the property and payroll fractions.
Footnote: 3 In 1995, the formula for calculating the allocation factor was modified to give double weight to the sales fraction. L. 1995, c. 245, § 1. Footnote: 4 The regulation refers to a substantial overlapping of employees and offices not officers. Compare N.J.A.C. 18:7-7.6(g)(3)(v) with New Jersey Division of Taxation, Technical Bulletin-3, issued June 2, 1991 and expiring June 30,1992. Footnote: 5 This Act, with a wide variety of amendments, has been adopted in twenty-four states and the District of Columbia, but not in New Jersey. The purpose of UDITPA was to establish a uniform method of division of income for tax purposes among the several taxing jurisdictions in order to assure that a taxpayer is not taxed on more than its net income. Unif. Div. of Income for Tax Purposes Act, Prefatory Note, 7 U.LA. 142 (2002). The Act is applicable to [a]ny taxpayer having income from business activity which is taxable both within and without [a] state. Id. § 2, at 155. The income allocated to a state equals the average of a property factor, payroll factor, and sales factor. Id. § 9, at 168.
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