In Re Par Pharmaceutical, Inc. Securities Litigation

733 F. Supp. 668, 1990 WL 34625
CourtDistrict Court, S.D. New York
DecidedMarch 21, 1990
Docket88 Civ. 8154 (RPP)
StatusPublished
Cited by69 cases

This text of 733 F. Supp. 668 (In Re Par Pharmaceutical, Inc. Securities Litigation) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Par Pharmaceutical, Inc. Securities Litigation, 733 F. Supp. 668, 1990 WL 34625 (S.D.N.Y. 1990).

Opinion

OPINION AND ORDER

ROBERT P. PATTERSON, Jr., District Judge.

Plaintiffs, asserting violations of the federal securities laws and RICO, bring this *672 class action on behalf of purchasers of the common stock of Par Pharmaceutical, Inc. (“Par”) during the period December 29, 1986 to April 18, 1989. 1 The class has yet to be certified. The defendants now move under Rules 12(b)(6) and 9(b) of the Federal Rules of Civil Procedure to dismiss the Consolidated Amended and Supplemental Class Action Complaint (“complaint”). 2

Plaintiffs are investors in Par, a corporation engaged in the manufacture and sale of generic drugs. Plaintiffs allegedly purchased Par’s stock at inflated prices because Par’s public statements and its filings with the Securities and Exchange Commission failed to disclose that Par and its subsidiary had made illegal payments to government officials to expedite approval of the companies’ applications for permission to manufacture certain drugs. After information concerning the alleged payments was publicly disclosed, the price of Par’s stock fell dramatically. Plaintiffs assert violations of Sections 10(b) and 20(a) of the Securities Exchange Act of 1934, 15 U.S.C. §§ 78j(b) and 78t(a), and Rule 10b-5 promulgated thereunder, violations of the Racketeer Influenced and Corrupt Organizations Act (“RICO”), 18 U.S.C. §§ 1962(c), (d), and common law fraud, deceit and negligent misrepresentation.

I. BACKGROUND

Defendant Par is a corporation in the business of manufacturing and marketing prescription and over the counter oral and topical generic drugs. Par owns 60% of a subsidiary, Quad Pharmaceutical, Inc. (“Quad”), which manufactures and markets injectable generic drugs. The individual defendants Perry Levine, Ashok Patel (“A. Patel”), R.K. Patel and Jacob Robbins (collectively the “Director Defendants”) constituted the entire Board of Directors of Par from the beginning of the alleged class period until December, 1988. All except Robbins were also officers of Par. 3 Defendant Dilip P. Shah was President and Chief Executive Officer of Quad from April 1985 until July 14, 1989, and was responsible for all regulatory aspects of Quad’s product development. Complaint at ¶¶ 6-14.

In connection with their businesses, Par and Quad are required to obtain approval of their products from the Food and Drug Administration (“FDA”). As a prerequisite for FDA approval, Par and Quad must demonstrate that their manufacturing facilities meet FDA requirements and that their generic drug products are safe and effective. Id. at ¶¶ 33-37.

The 62-page complaint alleges that, as with all generic drug companies, Par’s financial well being was dependent upon its ability to obtain continually first or early FDA approval for new products, and that defendants were “well aware of the necessity for expediting FDA approval of new Products.” 4 Id. at H¶ 39-40.

According to the complaint, defendants A. Patel and Shah made a series of 14 illegal payments to two FDA employees, beginning some time in 1986 and continuing until March, 1988, for the purpose of *673 securing expedited approval of Par products and to delay the approval of competing products. It is further alleged that the bribery scheme allowed Par to obtain FDA approval for the manufacture of a number of generic products before certain of its competitors. Id. at MI 56-65.

All of the defendants allegedly “were aware of the bribery scheme and its potential consequences or recklessly disregarded its existence.” Id. at 11 88. In support of this contention, the complaint asserts that Quad and/or Par, Levine, R.K. Patel and Robbins “delegated full authority” to A. Patel and Shah “to determine Par’s course of conduct concerning the company’s activities in regard to obtaining expedited approval from the FDA of Par Products.” Id. The complaint also states that Par and the Director Defendants, as a matter of company policy, “developed, refined, supervised, implemented and/or acquiesced to the bribery scheme ...,” and calls defendants Quad and Shah “knowing and direct participants in the bribery scheme.” Id. at 11124-125.

Plaintiffs also allege that, in conjunction with the bribery scheme, the defendants determined to create the illusion within the investment community that Par had a special expertise in obtaining expeditious FDA approvals of its products and that this expertise would result in continued growth and income. Their purpose was to inflate artificially the price of Par’s common stock. Id. at II123.

To that end, it is alleged, defendants falsely represented, in a series of public filings and other public statements during 1987 and 1988, that the company’s ability to secure speedy FDA approval for its products was because of Par’s “legitimate business acumen and ingenuity,” rather than the illegal payments, and failed to disclose that projections of Par’s future prospects “were based on past illegal activities” that, once revealed, “could not be sustained,” and that subjected Par to the “prospect of serious criminal penalties and sanctions.” Id. at 1167-90.

In June 1988, three months after the illegal payments to FDA officials stopped, the United States Congress began an investigation of the generic drug approval process at the FDA. On July 5, 1988, records of Par were subpoenaed in connection with that investigation. Par did not disclose this event, or make any reference to the alleged bribery scheme, in its July 1988 10-Q. Id. at 111192-93.

On August 15, 1988, Par disseminated its July 1988 Quarterly Report, which acknowledged the fact of the congressional investigation, but stated that “we are not aware of any instances of the favoritism that has been alleged in the investigation.” Id. at 1111 94-95.

On October 21, 1988, Par issued a press release stating that it had been informed by the United States Attorney in Maryland that Par, Quad and one of Quad’s executives were “targets” in an ongoing Grand jury investigation relating to improper payments to employees of the FDA’s generic drug division, and went on to say that Par “had no reason to believe that this matter would have any immediate impact upon its business or that of Quad.” Id. at ¶¶ 95-96. 5

In April 1989, A. Patel and Shah agreed to plead guilty in connection with the grand jury investigation. 6 In July 1989, Par and *674

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Bluebook (online)
733 F. Supp. 668, 1990 WL 34625, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-par-pharmaceutical-inc-securities-litigation-nysd-1990.