Item 1.01 | Entry Into a Material Definitive Agreement. |
On April 15, 2019, Recro Pharma, Inc., through its wholly-owned subsidiary, Recro Gainesville LLC (collectively, the “Company”) entered into Supplemental Agreement No. 3 to the Amended and Restated License and Supply Agreement (the “Supplemental Agreement”) with Watson Laboratories, Inc. (“Watson”), a subsidiary of Teva Pharmaceutical Industries Ltd., effective as of January 1, 2019.
Pursuant to the Amended and Restated License and Supply Agreement entered into on June 26, 2003 by and between Watson and the Company’spredecessor-in-interest Elan Corporation, plc (as supplemented by Supplemental Agreement No. 1, dated December 8, 2004, Supplemental Agreement No. 2, dated January 17, 2014 and the Supplemental Agreement, the “Agreement”), the Company is the exclusive supplier of VERAPAMIL SR (the “Product”), for which the Company holds the New Drug Application (“NDA”), to Watson and Watson has an exclusive license to package, import, use, offer for sale and sell the Product in the United States.
The Supplemental Agreement provides for a newsix-year term which will expire on December 31, 2024 (the “Initial Term”) after which the Agreement will automatically renew for additionalone-year periods (each a “Renewal Term”) unless the Agreement is (1) terminated by either party, or (2) not renewed by either party, by giving written notice at least eighteen months prior to the end of the Initial Term or any Renewal Term.
The foregoing description of the Supplemental Agreement does not purport to be complete and is qualified in its entirety by reference to the Supplemental Agreement, a copy of which is filed as Exhibit 10.1 and incorporated herein by reference.
Item 9.01 | Financial Statements and Exhibits. |
(d) Exhibits
* | Certain identified information in the exhibit has been omitted because it is both (i) not material and (ii) would likely cause competitive harm to the Company if publicly disclosed. |
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