Israeli generics giant Teva Pharmaceutical Industries (Teva) and Japan-based Takeda Pharmaceutical (Takeda) announced on 30 November 2015 that they had made a partnership to provide generics in Japan.
Teva and Takeda partner for generics in Japan
Home/Pharma News
|
Posted 11/12/2015
0
Post your comment

The joint venture will market Teva’s generics and Takeda’s off-patent drugs in Japan. It will operate as an independent company with its own Board of Directors, Chief Executive Officer, and Executive Leadership team and is expected to start operating in the second quarter of 2016. The two companies will split ownership 51% for Teva and 49% for Takeda.
The partners said the new venture will combine Teva’s generics portfolio with Takeda’s Japanese distribution network and brand recognition. They added that the business model is in line with the Japanese Government’s push to limit healthcare spending by increasing market penetration for generics. In response to the high amount of spending on medicines in Japan [1], the government has set the objectives to reach 80% generics penetration by the end of 2020.
Related article
Europe–Japan cooperation on generics and biosimilars regulation
Reference
1. GaBI Online - Generics and Biosimilars Initiative. Prescribing and dispensing generics in Japan [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2015 Dec 11]. Available from: www.gabionline.net/Generics/Research/Prescribing-and-dispensing-generics-in-Japan
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2015 Pro Pharma Communications International. All Rights Reserved.
Source: Takeda, Teva
Guidelines
FDA issues guidance on AI use in drug and biologicals regulatory decision making
ICH adopts Good Clinical Practice Guideline for clinical trials
Policies & Legislation
NPRA Malaysia trials new timelines for variation applications
Regulatory evolution and impact of simplified requirements for interchangeable biosimilars in the US
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
Bio-Thera partners with Tabuk in Saudi Arabia and SteinCares in LATAM
Klinge-Teva and MS Pharma agreements for Eylea and Stelara biosimilars in Europe and MENA
Biosimilars thrive as China’s biotech industry gains momentum
Greener Pharmaceuticals: WHO's call for innovative regulatory practices and eco-friendly innovations
Bio-Thera partners with Tabuk in Saudi Arabia and SteinCares in LATAM

Home/Pharma News Posted 18/02/2025
Klinge-Teva and MS Pharma agreements for Eylea and Stelara biosimilars in Europe and MENA

Home/Pharma News Posted 06/02/2025
Greener Pharmaceuticals: WHO's call for innovative regulatory practices and eco-friendly innovations

Home/Pharma News Posted 15/01/2025
The best selling biotechnology drugs of 2008: the next biosimilars targets

Post your comment