ARTICLE
9 November 2023

Cost Of Hatch-Waxman Litigation Decreases (Via Tax Deduction)

AV
Axinn Veltrop & Harkrider

Contributor

Axinn combines the skills, experience and dedication of the world’s largest firms with the focus, responsiveness, efficiency and attention to client needs of the best boutiques. The firm was established with a common vision: provide the highest level of service and strategic acumen in antitrust, intellectual property and high-stakes litigation.
As Benjamin Franklin famously remarked, "nothing is certain except death and taxes." Recently, the U.S. Court of Appeals for the Third Circuit provided more certainty...
United States Intellectual Property
To print this article, all you need is to be registered or login on Mondaq.com.

As Benjamin Franklin famously remarked, "nothing is certain except death and taxes." Recently, the U.S. Court of Appeals for the Third Circuit provided more certainty about the latter by holding that legal expenses incurred by generic drug manufacturers in defending patent infringement suits brought under the Hatch-Waxman Act are deductible from the manufacturers' federal taxes as ordinary and necessary business expenses. Mylan, Inc. & Subsidiaries v. Comm'r of Internal Revenue, 76 F.4th 230 (3d Cir. 2023).

In the appeal, the Commissioner of Internal Revenue argued that these expenses should be capitalized, under 26 U.S.C. § 263 and the associated regulations, as amounts paid to acquire approvals from the Food and Drug Administration ("FDA"). Id. at 243. The Third Circuit rejected the Commissioner's argument noting that "ultimate FDA approval is never decided by the outcome of patent litigation under [35 U.S.C.] § 271(e)(2), even if it is delayed by such litigation." Id. at 244. The Third Circuit concluded that "it makes no difference in deciding the question of deductibility whether the patent litigation expenses are incurred by the patentee or the alleged infringer. Nor does it matter that the deductibility question arises in the context of an ANDA suit." Id. at 239-240.

Generic drug manufacturers can certainly leverage this ruling at corporate tax time. Companies should also consult with their tax advisors about the treatment of costs associated with the preparation, assembly, and transmittal of notice letters required by the Abbreviated New Drug Application.

www2.ca3.uscourts.gov/...

The content of this article is intended to provide a general guide to the subject matter. Specialist advice should be sought about your specific circumstances.

We operate a free-to-view policy, asking only that you register in order to read all of our content. Please login or register to view the rest of this article.

See More Popular Content From

Mondaq uses cookies on this website. By using our website you agree to our use of cookies as set out in our Privacy Policy.

Learn More