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Biovail Corporation Announces Increase in Its Normal Course Issuer Bid.


Business Editors

TORONTO--(BW HealthWire)--May 31, 2002

Biovail Corporation (NYSE NYSE

See: New York Stock Exchange
:BVF BVF Biovail Corporation (stock symbol)
BVF Berufsverband der Frauenärzte eV (Muenchen, Germany)
BVF Bearing Versus Frequency
) (TSX TSX Toronto Stock Exchange (TSE before April, 2002)
TSX Transfer from Stack Pointer to Index
TSX True Space Extension
:BVF) today announced that the Company has authorized an increase in the number of common shares of the Company which may be repurchased under its normal course issuer bid. The Company initiated the bid on the New York Stock Exchange New York Stock Exchange (NYSE)

World's largest marketplace for securities. The exchange began as an informal meeting of 24 men in 1792 on what is now Wall Street in New York City.
 in February, 2002. Since this date, the Company has purchased 7,791,400 common shares through open market transactions on the New York Stock Exchange. The number of shares which may be purchased under the bid has now been increased to 12,862,800 common shares being 10% of the public float of the outstanding common shares of the Company at the date of the commencement of the bid. The common stock will be purchased through transactions on the Toronto Stock Exchange Toronto Stock Exchange (TSE)

Canada's largest stock exchange, trading approximately 1,200 company stocks and 33 options.
 and the New York Stock Exchange in accordance with applicable rules and regulations. Purchases may be made commencing June 4, 2002. The bid will expire on February 14, 2003.

Biovail Corporation is a full-service pharmaceutical company, engaged in the formulation, clinical testing, registration, manufacture, sale and promotion of pharmaceutical products utilizing advanced drug delivery technologies. Additional information about Biovail may be found at the Company's website at http://www.biovail.com.

"Safe Harbor" statement under the Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and  of 1995.

To the extent any statements made in this release contain information that is not historical, these statements are essentially forward looking and are subject to risks and uncertainties, including the difficulty of predicting FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
 approvals, acceptance and demand for new pharmaceutical products, the impact of competitive products and pricing, new product development and launch, reliance on key strategic alliances, availability of raw materials, the regulatory environment, fluctuations in operating results and other risks detailed from time to time in the company's filings with the Securities and Exchange Commission.
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Publication:Business Wire
Date:May 31, 2002
Words:306
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