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Re: License and Supply Agreement

License Agreement

Re: License and Supply Agreement | Document Parties: CORNERSTONE THERAPEUTICS INC | Cornerstone Biopharma Inc. | MEIJI SEIKA KAISHA, LTD. You are currently viewing:
This License Agreement involves

CORNERSTONE THERAPEUTICS INC | Cornerstone Biopharma Inc. | MEIJI SEIKA KAISHA, LTD.

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Title: Re: License and Supply Agreement
Date: 11/5/2008
Industry: Biotechnology and Drugs     Sector: Healthcare

Re: License and Supply Agreement, Parties: cornerstone therapeutics inc , cornerstone biopharma inc. , meiji seika kaisha  ltd.
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Exhibit 10.8

MEIJI SEIKA KAISHA, LTD. INTERNATIONAL HEADQUARTERS, PHARMACEUTICALS

 

 

 

4-16, Kyobashi 2 Chome, Chuo-ku, Tokyo, 104-8002 Japan

 

TELEPHONE: +81-3-3273-3426 FAX: +81-3-3281-4058

July 27, 2007

Cornerstone Biopharma Inc.
2000 Regency Parkway
Suite 255
Cary, North Carolina 27511
U.S.A.

Re: License and Supply Agreement

This letter is to confirm the mutual understanding and agreement between Meiji Seika Kaisha, Ltd. (“Meiji”) and Cornerstone Biopharma Inc. (“Cornerstone”) with respect to the License and Supply Agreement dated October 12, 2006 regarding Cefditoren Pivoxil as amended by the Amendment No. 1 dated July 27, 2007 (the “License Agreement”).

1. Capitalized terms not defined herein shall have the meanings ascribed to them in the License Agreement.

2. Tedec-Meiji Farma S.A. (“Tedec-Meiji”) shall be added as a production site for production of 200mg oral tablet form of the Product to be specified in the Product Registrations of that Product. Cornerstone undertakes to do all regulatory works and filings required to add Tedec-Meiji as a production site specified in the Product Registrations of 200mg oral tablet form of the Product and Meiji shall provide Cornerstone with all information and data required for such purpose. Meiji shall pay to Cornerstone US$349,000 as reimbursement for expenses to be incurred by Cornerstone for regulatory works and filings required to add Tedec-Meiji as a production site. Meiji’s burden for expenses for regulatory works and filings required to add Tedec-Meiji as a production site shall be limited to this payment of US$349,000. This payment of US$349,000 shall be made by way of several installments to be mutually agreed between Meiji and Cornerstone and shall be completed no later than June 30, 2008.

3. Meiji hereby grants Cornerstone an exclusive right to develop, and apply for and obtain the Product Registrations for, 400mg oral tablet form of the Product (“400mg Product”). Tedec-

 

[***] Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission

 


 

MEIJI SEIKA KAISHA, LTD. INTERNATIONAL HEADQUARTERS, PHARMACEUTICALS

 

 

 

4-16, Kyobashi 2 Chome, Chuo-ku, Tokyo, 104-8002 Japan

 

TELEPHONE: +81-3-3273-3426 FAX: +81-3-3281-4058

Meiji shall be designated as the production site for production of the 400mg Product to be specified in the Product Registrations of the 400mg Product. All expenses required to develop

and obtain the Prod


 
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