Case Information
*1
In the
United States (Gourt of Appeals
For the Circuit
No. 12-2977 UNITED FOOD AND COMMERCIAL WORKERS UNIONS AND EMPLOYERS Midwest Health Benefits Fund, individually and on behalf of all others similarly situated,
Plaintiffs-Appellants, v.
WALGREEN CO., PAR Pharmaceutical COS., Inc., and Par Pharmaceutical, Inc.,
Defendants-Appellees.
Appeal from the United States District Court for the Northern District of Illinois, Eastern Division.
No. 12 C 204āSamuel Der-Yeghiayan, Judge.
ARGUED JANUARY 24, 2013āDECIDED JULY 8, 2013
Before Manion and wood, Circuit Judges, and BARKER, District Judge.*
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WOOD, Circuit Judge. The United Food and Commercial Workers Unions and Employers Midwest Health Benefits Fund (the Fund), an employee benefit plan that provides healthcare benefits to its participants, is convinced that the Walgreen Company (Walgreens) fraudulently overcharged it and other insurance providers by filling prescriptions for several generic drugs with a dosage form that differed from, and was more expensive than, the dosage form prescribed to the customer. The Fund filed suit against Walgreens, as well as Par Pharmaceutical Companies and Par Pharmaceutical, Inc. (collectively Par), which manufactured the generic drugs at issue, alleging that the defendants engaged in a scheme to defraud insurers. This scheme, the Fund concludes, violated the Racketeer Influenced and Corrupt Organizations Act (RICO), 18 U.S.C. §§ 1961-1968. Finding that the complaint failed to state a claim upon which relief could be granted, the district court dismissed the case.
We affirm. While the complaint contains ample allegations of misconduct by both Walgreens and Par, it falls short of plausibly alleging the type of concerted activity undertaken on behalf of an identifiable enterprise necessary to a successful RICO claim. RICO is not violated every time two or more individuals commit one of the predicate crimes listed in the statute. In the end, that is all that this complaint alleges, and thus the action was properly dismissed.
I
As this case reaches us on appeal from a motion to dismiss, we accept all facts alleged in the complaint as
*3 true. Par is the fifth-largest generic drug manufacturer in the United States. In the late 1990s it began to manufacture a generic version of the drug ranitidine, which is marketed under the brand name Zantac and which went off-patent in 1997. Although ranitidine is most commonly prescribed as either or tablets, Par (as well as several other manufacturers) manufactured ranitidine in capsule form. While tablets and capsules of a given drug contain the same active ingredient, the federal Food and Drug Administration (FDA) does not consider the different dosage forms to be "bioequivalent." (It has held this position since at least December 2000.) As a result, a prescription for ranitidine tablets may not be filled with ranitidine capsules (or vice versa) without authorization from the prescribing physician.
In the early 2000s Par began to market and distribute a generic version of fluoxetine, which is sold under the brand name Prozac and which went off-patent in 2001. Most fluoxetine is prescribed as or capsules; Par, however, had marketing and distribution rights to and fluoxetine tablets. As with ranitidine, prescriptions for fluoxetine capsules may not be filled with fluoxetine tablets in the absence of a physician's authorization.
Although Par's ranitidine capsules and fluoxetine tablets were considerably less popular than the alternative dosage forms, they had the potential to be much more lucrative. To understand why, a brief discussion of pharmacy reimbursement practices is in order. When a patient seeking to fill a prescription has insurance,
*4 the pharmacy recoups most of the cost of filling that prescription from the insurer. The insurer could be the government, a private insurance company, or, as in this case, a welfare-benefit fund. Each insurer (or, more generically, Third-Party Payor (TPP)) establishes the rates at which it will reimburse the pharmacy. For generic drugs that are available from multiple sources (most of them), the reimbursement rate is calculated as a Maximum Allowable Cost, which represents the maximum amount that the TPP will reimburse the pharmacy for a given drug. Maximum Allowable Costs are set based on price information gathered in the marketplace. They reflect changing market conditions and bear a reasonable relation to drugs' actual costs. If, however, there are too few manufacturers of a given generic to determine a Maximum Allowable Cost, the reimbursement rate is set using an alternative measure: the Average Wholesale Price. Average Wholesale Prices are benchmark prices published by drug manufacturers; they often bear little to no relation to a drug's cost.
Unsurprisingly, TPP reimbursement rates are substantially higher when based on the Average Wholesale Price than when based on the Maximum Allowable Cost. A pharmacy makes more money on prescriptions reimbursed using Average Wholesale Prices, and this in turn enables the drug manufacturer to command higher prices for those drugs. Because so few manufacturers made either ranitidine capsules or fluoxetine tablets, reimbursement rates for those dosage forms of those drugs were calculated using the favorable Average Wholesale Price method. By contrast, the more popular
*5 ranitidine tablets and fluoxetine capsules were reimbursed according to the Maximum Allowable Cost method.
Par, realizing that the disparity between reimbursement formulas for the different dosage forms of ranitidine and fluoxetine presented an opportunity for profit, crafted a marketing pitch aimed at convincing pharmacies to purchase the more expensive dosage forms of each one. In presentations to pharmacies-including Walgreens, but also others, such as Caremark and CVS-Par highlighted the millions of dollars in additional profits the pharmacies stood to earn if they could find a way to fill their ranitidine and fluoxetine prescriptions with dosage forms reimbursed under the generous Average Wholesale Price formula. These presentations implied (at the least) that the pharmacies could legally fill prescriptions written for one dosage form with an alternative dosage form without seeking approval from the prescribing physician, a suggestion that directly contravened the FDA's position that the tablets and capsules are not bioequivalent.
Par's pitch evidently worked on Walgreens. Beginning in 2001, Walgreens reconfigured its internal computer systems so that all prescriptions for ranitidine were filled with capsules and all prescriptions for fluoxetine were filled with tablets, regardless of the dosage form actually prescribed. The Fund alleges that Walgreens's pharmacists implemented this switch without consulting the prescribing physicians. Worse, Walgreens's director of pharmacy marketing, Tom Lawlor, falsely represented in an email to company pharmacists that
*6 Par's ranitidine capsules were "AB-rated generic products" and thus could be substituted for ranitidine capsules under FDA regulations. Worse still, Walgreens continued its policy of automatically switching dosage forms even after receiving a rebuke from the Illinois Department of Public Health in July 2001, warning that the statement that ranitidine capsules were AB -rated generics was "false and deceptive."
Walgreens's dosage-form-switching practices eventually attracted scrutiny from a number of states' attorneys general and the Justice Department. In September 2004, acting on the advice of counsel, Walgreens ended the switching program for all new prescriptions and resumed filling ranitidine and fluoxetine prescriptions with the dosage form specified by the physician. Walgreens continued to fill existing prescriptions with the more expensive dosage forms for some unspecified period of time. Lawlor explained in an email that this change in policy was implemented "quietly." In order to offset the revenue loss from the termination of the switching program, Walgreens negotiated with Par to receive price reductions on ranitidine and fluoxetine.
In 2008, at the request of the United States, the court unsealed a qui tam complaint against Walgreens. The complaint alleged that the switching program resulted in overcharges to the federal government and various states in violation of both the False Claims Act (FCA), 31 U.S.C. , and related state laws. See Complaint, United States ex rel. Lisitza v. Walgreens Co., No. 03-cv-00744 (N.D. Ill. Jan. 31, 2003). Walgreens paid
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\ \ Million to U.S., Forty-Six States &; Puerto Rico to Settle Medicaid Prescription Drug Fraud Allegations, DEP'T OF JUSTICE (June 4, 2008), http://www.justice.gov/opa/pr/2008/June/ 08-civ-496.html. In 2011, a similar qui tam complaint against Par was unsealed. See Second Amended Complaint, United States ex rel. Lisitza v. Par Pharm. Co., No. 06-cv-06131 (N.D. Ill. July 19, 2011). That case is ongoing.
Relying largely on the pleadings and documents from the qui tam cases, the Fund filed this class action lawsuit in January 2012, alleging that Walgreens and Par conducted an association-in-fact RICO enterprise for the purpose of overcharging insurers by switching dosage forms of ranitidine and fluoxetine. Walgreens and Par moved to dismiss for failure to state a claim. The district court granted the motion after concluding, among other things, that the Fund failed to allege sufficiently that Walgreens and Par conducted the affairs of an enterprise within the meaning of 18 U.S.C. § 1962(c). The Fund appeals.
II
The district court identified numerous deficiencies in the Fund's complaint, each of which would provide an independent basis for dismissal. We need not be so comprehensive. Because we agree with the district court that the complaint fails to allege that Walgreens and Par "conduct[ed]" the affairs of an "enterprise," 18 U.S.C.
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§ 1962(c), we see no need to address the district court's alternative bases for dismissal.
We review de novo whether the Fund's enterprise allegations meet the pleading standards of Rule 8(a) of the Federal Rules of Civil Procedure. St. John's United Church of Christ v. City of Chi.,
A
Section 1962(c) makes it "unlawful for any person employed by or associated with any enterprise engaged in, or the activities of which affect, interstate or foreign commerce, to conduct or participate, directly or indirectly, in the conduct of such enterprise's affairs through a pattern of racketeering activity." Critically for our purposes, to state a claim under this section, a plaintiff must identify an "enterprise." See, e.g., Slaney v. Int'l Amateur Athletic Ass'n,
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other legal entity, and any union or group of individuals associated in fact although not a legal entity." 18 U.S.C.
1961(4). The Supreme Court has held on multiple occasions that this definition is to be interpreted broadly. See, e.g., Boyle v. United States,
Despite the expansive nature of this definition, it is not limitless. Section 1962(c) requires a plaintiff to identify a "person"-i.e., the defendant-that is distinct from the RICO enterprise. See Cedric Kushner Promotions, Ltd. v. King,
*10 may set those aside, as we need not reach this aspect of the district court's decision.)
The Fund points to Walgreens and Par as the "persons" it has identified for purposes of RICO, and it defines the "enterprise" as an entity consisting of Walgreens, Par, and management personnel from the two companies. According to the complaint, the members of the enterprise associated for the common purpose of profiting from illegally substituting Par's more expensive dosage forms of ranitidine and fluoxetine for the cheaper dosage forms actually prescribed. The complaint further alleges that communications between the parties, as well as Walgreens's implementation of the illegal dosage-form-switching program using Par's pills, establishes relationships among the enterprise's members. The scheme's multiyear duration, it concludes, establishes longevity. The Fund asserts that the enterprise was known as "Walgreens/Par/Hrp" (also referred to as the "Hrp enterprise"). It supports this terminology based on Par's use of this label in a PowerPoint slide accompanying a presentation it made to Walgreens regarding ranitidine.
Before Boyle, we would have had little trouble concluding that these allegations were insufficient to plead the existence of an association-in-fact distinct from Walgreens and Par. See, e.g., Stachon v. United Consumers Club, Inc.,
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such an association had to have certain structural features (a purpose, relationships among those associated with it, and adequate longevity), that the structure had to be ascertainable, but that no additional structural requirements could be inferred from the statute. Even if we were to assume, however, that the complaint sufficiently pleads the existence of an association-in-fact enterprise under Boyle, it does not adequately allege that Walgreens and Par were conducting the affairs of this "Hrp enterprise," as opposed to their own affairs. See Reves,
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prise members. And although it would be possible to envision a complaint that accused individual corporate personnel of improperly hijacking the business operations of their companies for illicit ends, see Jay E. Hayden,
To be sure, Walgreens and Par were not strangers. Representatives from the companies regularly communicated with one another, and Walgreens purchased its generic ranitidine and fluoxetine from Par. This type of interaction, however, shows only that the defendants had a commercial relationship, not that they had joined together to create a distinct entity for purposes of improperly filling ranitidine and fluoxetine prescriptions. See Crichton,
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Nor does the fact that Walgreens's and Par's activities were by all appearances illegal indicate that the companies were acting on behalf of a distinct enterprise. Cf. Baker,
The Fund asks us to assume that Walgreens and Par were acting on behalf of the supposed Hrp enterprise "because neither Defendant could have accomplished the [drug-switching] scheme[] on its own." The Fund reasons that because Walgreens does not manufacture drugs and Par does not fill prescriptions, neither company could have implemented the drug-switching scheme without the other. (This assumes, perhaps optimistically, a dearth of other market actors who might have been tempted to earn extra money this way.) It relies on
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the Third Circuit's decision in In re Insurance Brokerage Antitrust Litigation,
The Fund's reliance on Insurance Brokerage is inapt. For one thing, it is far from obvious that Walgreens could not have accomplished the drug-switching scheme on its own by simply purchasing expensive dosage forms from Par and other manufacturers (of which there were
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apparently several) and filling prescriptions with these expensive dosage forms on its own initiative. Moreover, in Insurance Brokerage, the defendants could not have achieved their goals-namely, fixing a competitive bidding process in order to win insurance contracts at inflated prices-without cooperation that fell outside the bounds of the parties' normal commercial relationships. Companies competing for business in a legitimate market that assigns business through bidding do not disclose their bids to one another in advance. By contrast, while it is true that Walgreens does not make drugs and Par does not fill prescriptions, and that the two companies must therefore "cooperate" in order for drugs to reach consumers, such cooperation describes virtually every prescription pharmaceutical distribution chain. The allegations in the complaint do not indicate how the cooperation in this case exceeded that inherent in every commercial transaction between a drug manufacturer and pharmacy, and without such an indication, we cannot find a basis for inferring that Walgreens and Par were conducting the enterprise's affairs.
B
The Fund's failure adequately to allege that Walgreens and Par conducted the affairs of an enterprise is also fatal to its RICO conspiracy claim. Proof of a conspiracy within the scope of RICO requires a showing that: " (1) the defendant agreed to maintain an interest in or control of an enterprise or to participate in the affairs of an enterprise through a pattern of racketeering activity, and (2) the
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defendant further agreed that someone would commit at least two predicate acts to accomplish those goals.'" DeGuelle v. Camilli,
The judgment of the district court is AFFIRMED.
NOTES
Notes
* The Honorable Sarah Evans Barker, United States District Court for the Southern District of Indiana, sitting by designation.
