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TERMINATION AGREEMENT

Termination Agreement

TERMINATION AGREEMENT | Document Parties: Noven Pharmaceuticals, Inc. | Endo Pharmaceuticals, Inc. You are currently viewing:
This Termination Agreement involves

Noven Pharmaceuticals, Inc. | Endo Pharmaceuticals, Inc.

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Title: TERMINATION AGREEMENT
Governing Law: New York     Date: 3/15/2006
Industry: Biotechnology and Drugs     Sector: Healthcare

TERMINATION AGREEMENT, Parties: noven pharmaceuticals  inc. , endo pharmaceuticals  inc.
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Exhibit 10.30

The confidential portions of this exhibit have been filed separately with the Securities and Exchange Commission pursuant to a confidential treatment request in accordance with Rule 24b-2 of the Securities and Exchange Act of 1934, as amended. REDACTED PORTIONS OF THIS EXHIBIT ARE MARKED BY AN ***.

TERMINATION AGREEMENT

     This Termination Agreement (“Termination Agreement”) is dated as of February 24, 2006, by and between Noven Pharmaceuticals, Inc., a Delaware corporation (“Noven”), and Endo Pharmaceuticals, Inc., a Delaware corporation (“Endo”). Noven and Endo are collectively referred to as “Parties” and individually as “Party.”

RECITALS

     WHEREAS, the Parties entered into an agreement dated February 25, 2004 (“License Agreement”) related to the exclusive distribution of certain fentanyl transdermal patch products (“Licensed Product”);

     WHEREAS, the Parties entered into a supply agreement dated as of February 25, 2004 ( “Supply Agreement”) and an intercompany quality control agreement dated as of February 25, 2004 ( “Quality Agreement”) relating to the Licensed Product;

     WHEREAS, the Parties further agreed that they would work together with respect to certain additional products using Noven’s transdermal patch technology (“Additional Products”), as more particularly described in the License Agreement;

     WHEREAS, the Food & Drug Administration (“FDA”) advised Noven on September 27, 2005 that the FDA would not approve the Licensed Product based on the FDA’s assessment of potential safety concerns related to the higher drug content in the Licensed Product;

     WHEREAS, the Parties mutually desire to terminate the Supply Agreement and Quality Control Agreement and wish to terminate the License Agreement with respect to the Licensed Product as set forth below; and

     WHEREAS, the Parties desire that the License Agreement survive with respect to the Additional Products, with certain modifications as described herein; and

     WHEREAS, this Agreement memorializes the understandings of the parties with respect to the subject matter hereof as of December 31, 2005 (the “Effective Date”).

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     NOW, THEREFORE, in consideration of the foregoing premises, and of the mutual promises and covenants contained in the Termination Agreement, and for other good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, Noven and Endo agree as follows:

Article 1. Definitions.

     Capitalized terms used herein shall have the meaning as provided in the License Agreement, unless as otherwise set forth below.

Article 2. Termination of Rights and Obligations with Respect to Licensed Product.

     2.1 Generally. The Parties mutually agree to, and hereby do, terminate in their entirety the Supply Agreement and the Quality Agreement, and all of the Parties’ respective rights and obligations thereunder, if any, shall terminate as of the Effective Date. Except as explicitly provided in this Termination Agreement, all of the Parties’ respective rights and obligations with respect to Licensed Product under the License Agreement, if any, shall terminate; provided, that all of the Parties’ rights and obligations under the License Agreement with respect to any Additional Product(s) shall continue. By way of clarification of the preceding sentence, on and after the date hereof Section 13.03 of the License Agreement (including Section 13.03(b) with respect to the Licensed Products) shall survive a


 
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