From Casetext: Smarter Legal Research

Apotex v. Drug Admin

United States Court of Appeals, District of Columbia Circuit
Feb 23, 2007
226 F. App'x 4 (D.C. Cir. 2007)

Summary

holding that Chevron deference applies to FDA's statutory interpretation of the FDCA announced through informal adjudication

Summary of this case from Aqua Prods., Inc. v. Matal

Opinion

No. 06-5060.

February 23, 2007.

Appeal from the United States District Court for the District of Columbia, (No. 05cv00125).

Arthur Ya-Shih Tsien, Olsson, Frank Weeda, Washington, DC, Christine J. Siwik, William Andrew Rakoczy, Rakoczy Molino Mazzochi Siwik LLP, Chicago, IL, for Appellant.

Eric Michael Blumberg, Food Drug Administration, Rockville, MD, Eugene M. Thirolf, Jr., Andrew E. Clark, Attorney, Douglas William Steam, U.S. Department of Justice, Office of Consumer Litigation, Daniel Meron, General Counsel, U.S. Department of Health Human Services, Office of General Counsel, Peter Douglas Keisler, U.S. Department of Justice, Office of the Deputy Atty. Gen., Washington, DC, for Appellees.

Before: GINSBURG, Chief Judge, and GRIFFITH, Circuit Judge, and SILBERMAN, Senior Circuit Judge.


JUDGMENT


This appeal was considered on the record from the United States District Court for the District of Columbia and on the briefs and arguments by the parties. The Court has determined that the issues presented occasion no need for an opinion. See D.C. Cir. R. 36(b). It is

ORDERED AND ADJUDGED that the judgment of the district court — accompanied by its thoughtful opinion — is affirmed. We add only two points. The first is that the district judge's opinion, which grants Chevron deference to the FDA's statutory interpretation of 21 U.S.C. § 355(j)(5)(B)(iv) embodied in FDA approval letters (i.e., informal adjudications), is supported by the Supreme Court's post-Mead decision in Barnhart v. Walton, 535 U.S. 212, 222, 122 S.Ct. 1265, 152 L.Ed.2d 330 (2002), as well as our own decision in Mylan Laboratories, Inc. v. Thompson, 389 F.3d 1272, 1279-SO (D.C. Cir. 2004). Moreover, the FDA's interpretation of 21 U.S.C. § 355(j)(5)(B)(iv) is clearly supported by its regulation, 21 C.F.R. § 314.107(c)(1), which also warrants Chevron deference under United States v. Mead Corp., 533 U.S. 218, 121 S.Ct. 2164, 150 L.Ed.2d 292 (2001).

Pursuant to D.C. Circuit Rule 36, this disposition will not be published. The Clerk is directed to withhold issuance of the mandate herein until seven days after resolution of any timely petition for rehearing or rehearing en banc. See Fed.R.App.P. 41(b); D.C. Cir. Rule 41.


Summaries of

Apotex v. Drug Admin

United States Court of Appeals, District of Columbia Circuit
Feb 23, 2007
226 F. App'x 4 (D.C. Cir. 2007)

holding that Chevron deference applies to FDA's statutory interpretation of the FDCA announced through informal adjudication

Summary of this case from Aqua Prods., Inc. v. Matal
Case details for

Apotex v. Drug Admin

Case Details

Full title:APOTEX, INC., Appellant v. FOOD DRUG ADMINISTRATION, et al., Appellees

Court:United States Court of Appeals, District of Columbia Circuit

Date published: Feb 23, 2007

Citations

226 F. App'x 4 (D.C. Cir. 2007)

Citing Cases

Mylan Pharms., Inc. v. U.S. Food & Drug Admin.

On appeal, the Court of Appeals for the District of Columbia lauded the district judge's “thoughtful…

Apotex Inc. v. Eisai Inc.

Accordingly, once a first-filer obtains this marketing exclusivity, the commencement of the 180-day period…