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EISAI CO., LTD. v. DR. REDDY'S LABORATORIES, LTD.

Nos. 03 Civ. 9053(GEL), 03 Civ. 9223(GEL).

472 F.Supp.2d 493 (2006)

EISAI CO., LTD. and Eisai Inc., Plaintiffs, v. DR. REDDY'S LABORATORIES, LTD., Dr. Reddy's Laboratories, Inc., Defendants. Eisai Co., Ltd. and Eisai Inc., Plaintiffs, v. Teva Pharmaceuticals USA, Inc., Defendant.

United States District Court, S.D. New York.

October 6, 2006.

Attorney(s) appearing for the Case

Robert L. Baechtold, Joseph M. O'Malley, Bruce M. Wexler, Fitzpatrick, Cella, Harper & Scinto, New York, NY; David B. Tulchin, James T. Williams, and Bradley A. Harsch, Sullivan & Cromwell LLP, New York, NY, for Plaintiffs.

Maurice B. Ross, Louis H. Weinstein, Ellen T. Lowenthal, Nathaniel I. Watts, Budd Larner, P.C., Short Hills, NJ, for Defendants Dr. Reddy's Laboratories, Ltd. and Dr. Reddy's Laboratories Inc.

David M. Hashmall, Frederick H. Rein, and Elaine Herrmann Blais, Goodwin Proctor LLP, New York, NY, for Defendant Teva Pharmaceuticals USA, Inc.

OPINION AND ORDER

LYNCH, District Judge.

The Hatch-Waxman Act, 21 U.S.C. § 355 and 35 U.S.C. § 271(e) (1994) (codified as amended), permits would-be manufacturers of generic versions of an already approved, patented drug to seek expedited approval from the Food and Drug Administration ("FDA") before expiration of the patent, by means of an Abbreviated New Drug Application ("ANDA"). See Yamanouchi Pharmaceutical Co., Ltd. v. Danbury Pharmacal...

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