Ortho-McNeil Pharmaceutical, Inc. v. Mylan Laboratories Inc.

569 F.3d 1353, 91 U.S.P.Q. 2d (BNA) 1274, 2009 U.S. App. LEXIS 16561, 2009 WL 1606944
CourtCourt of Appeals for the Federal Circuit
DecidedJune 10, 2009
Docket2008-1600
StatusPublished
Cited by7 cases

This text of 569 F.3d 1353 (Ortho-McNeil Pharmaceutical, Inc. v. Mylan Laboratories Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Ortho-McNeil Pharmaceutical, Inc. v. Mylan Laboratories Inc., 569 F.3d 1353, 91 U.S.P.Q. 2d (BNA) 1274, 2009 U.S. App. LEXIS 16561, 2009 WL 1606944 (Fed. Cir. 2009).

Opinion

DYK, Circuit Judge.

Defendants-Appellants Mylan Laboratories and Mylan Pharmaceuticals (collec *1355 tively “Mylan”) appeal from the district court’s order awarding approximately $1.3 million in costs to Plaintiff-Appellee Daiichi Pharmaceutical Co. (“Daiiehi”) under 28 U.S.C. § 1920 and Federal Rule of'Civil Procedure 54(d). We affirm-in-part, vacate-in-part, and remand.

BACKGROUND

This appeal concerns an award of costs stemming from a patent dispute. Daiiehi is the owner of U.S. Patent No. 5,053,407, which is directed to an antibiotic compound known as levofloxacin. Levofloxacin is a pioneer drug registered with and approved by the United States Food and Drug Administration under the trade name “Levaquin.” Ortho-McNeil Pharm., Inc. v. Mylan Labs., Inc., 267 F.Supp.2d 533, 536 (N.D.W.Va.2003). In November 2001, Mylan submitted an abbreviated new drug application to the Food and Drug Administration seeking approval to manufacture and sell levofloxacin tablets, together with a so-called “Paragraph IV” certification contending that Daiichi’s patent was invalid. See 21 U.S.C. § 355(j)(2)(A)(vii)(IV). Daiiehi brought a Hatch-Waxman infringement suit against Mylan. 1 See 35 U.S.C. § 271(e)(2). Mylan asserted that Daiichi’s patent was invalid or unenforceable on several grounds. The district court found that Mylan had failed to prove any of its invalidity or unenforceability contentions by clear and convincing evidence, and we affirmed. Ortho-McNeil Pharm., Inc. v. Mylan Labs., Inc., No. 1:02-CV-32, 2005 WL 41648, at *1 (N.D.W.Va. Jan. 4, 2005), aff’d, 161 Fed.Appx. 944, 945 (Fed. Cir.2005); see also Ortho-McNeil Pharm., Inc. v. Mylan Labs., Inc., 348 F.Supp.2d 713, 764 (N.D.W.Va.2004).

As the prevailing party in the action, Daiiehi submitted to the district court a bill of costs pursuant to Federal Rule of Civil Procedure 54(d) 2 and 28 U.S.C. § 1920 seeking approximately $2.2 million from Mylan. Mylan raised numerous objections to Daiichi’s bill of costs, including the argument that certain discovery had been conducted jointly for this action and a separate levofloxacin-related civil action against Teva Pharmaceuticals, Inc. in a different district court, and that costs of the discovery should be apportioned between the two actions.

On August 18, 2008, the district court entered a thirty-one page “Order Reducing Daiichi’s Bill of Costs and Awarding Costs” awarding costs to Daiiehi, but in a lesser amount than sought by Daiiehi. Ortho-McNeil, No. 1:02-CV-32, slip op. at 1 (N.D.W.Va. Aug. 18, 2008) (“Order”). After reducing Daiichi’s requested costs by approximately 40% (including most notably a substantial reduction in translation costs awarded), the district court awarded costs, which are summarized as follows:

Fees of Clerk.....................$ 75.00
Service of summons & subpoena.....$ 1,676.81
Court reporter fees:
Trial transcripts...............$ 31,225.18
Pre-trial healing transcripts ... .$ 4,924.20
Deposition transcripts..........$ 112,911.70
Witness fees......................$ 53,939.94
Exemplification & copying fees......$ 89,424.20
Interpretation ....................$ 24,512.36
Translation.......................$1,011,712.00
Total ............................$1,330,401.39

*1356 Order, slip op. at 30-31. -In addition, the district court rejected Mylan’s - argument that discovery costs should be allocated between its case and the Teva action, noting that “no deposition at issue ... was undertaken by Teva solely for use in that case” without also being necessary for Mylaris case. Id. at 29. Mylan timely appealed, and we have jurisdiction under 28 U.S.C. § 1295(a)(1).

DISCUSSION

We apply the law of the regional circuit, here the Fourth Circuit, in reviewing the award of costs under Rule 54(d) and 28 U.S.C. § 1920. See Summit Tech., Inc. v. Nidek Co., 435 F.3d 1371, 1374 (Fed.Cir.2006). Under Fourth Circuit law, Rule 54(d) “creates the presumption that costs are to be awarded to the prevailing party,” and we review a district court’s award of costs for abuse of discretion. Cherry v. Champion Int’l Corp., 186 F.3d 442, 446 (4th Cir.1999).

On appeal, Mylan essentially restates many of the same arguments it made to the district court opposing Daiichi’s bill of costs. With regard to the large majority of the costs, we see no basis to disturb the judgment of the district court. Thus, we affirm the district court’s award of translation costs for potential trial exhibits, translation costs for privilege log documents, and other costs not discussed below.

One issue, however, requires further discussion. The district court here rejected Mylan’s argument that the joint discovery costs should have been apportioned between this action and the parallel levofloxacin case in the District of New Jersey brought against Teva. Order, slip op. at 29-30; see Ortho-McNeil Pharm., Inc. v. Teva Pharms. USA, No. 3:02-CV-02794 (D.N.J. filed June 12, 2002). On appeal Mylan argues that this was erroneous.

Although no formal joint-discovery agreement appears to have been entered on the docket of either court, the parties do not dispute that for Daiichi’s convenience the depositions of Daiichi’s witnesses were in fact taken jointly by Mylan and Teva, with attorneys for both Mylan and Teva present, and with the captions of both cases on the transcripts. In other words, the depositions were formally taken in both cases. There is also no dispute that the depositions at issue were necessary in both cases. Indeed, Daiichi admits that the New Jersey district court could have properly taxed the deposition costs, and it acknowledged at oral argument that, had the New Jersey district court done so, Daiichi could not have also recovered those same costs in this action.

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569 F.3d 1353, 91 U.S.P.Q. 2d (BNA) 1274, 2009 U.S. App. LEXIS 16561, 2009 WL 1606944, Counsel Stack Legal Research, https://law.counselstack.com/opinion/ortho-mcneil-pharmaceutical-inc-v-mylan-laboratories-inc-cafc-2009.