Sawai Pharmaceutical Company Ltd (Sawai) has signed an agreement to purchase the generics section of US firm Upsher-Smith in an attempt to enter the vast American pharmaceuticals market.
Japan’s Sawai to acquire US generics business Upsher-Smith
Home/Pharma News | Posted 19/05/2017 0 Post your comment
Sawai is a leading Japanese generic drug manufacturer, based in Osaka. Like many Japanese firms, Sawai is focused on providing a stable supply of generics for the country. Due to an ageing population and the rising costs of medicines, the Japanese Government aims to increase the share of generics prescriptions. In August 2016, Sawai produced a business plan announcing its aim to maintain its strong position as a manufacturer of generic medicines and to help meet the government’s goal of reaching an 80% share of generics prescriptions by 2020. The business plan also described Sawai’s intention to target the US for expansion.
Upsher-Smith is a privately owned pharmaceutical company based in Minnesota, USA. The company has a product portfolio of over 30 pharmaceuticals, mainly oral solid preparations, as well as a 30 drug-strong pipeline.
Under the agreement signed on the 20 April 2017, Sawai will buy all equity interest in Upsher-Smith’s generics business from its parent company Acova, for the sum of US$1.05 billion. Upsher-Smith’s non-generic pharmaceutical activity however will remain under Acova.
The acquisition is expected to complete in June 2017, subject to regulatory approval, and will increase Sawai’s presence in the US market. The company say they aim to build a US business which combines their research and development capabilities with Upsher-Smith’s distribution network, commercial relationships and respected brand. Sawai’s President Mitsuo Sawai said they are delighted to sign the agreement with Upsher-Smith, who are also a family-owned generics firm.
Related articles
Approaches to assure quality and improve patient perceptions of 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 © 2017 Pro Pharma Communications International. All Rights Reserved.
Source: Reuters
Guidelines
Regulatory update for post-registration of biological products in Brazil
New regulations in Brazil for the registration of biosimilars
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
Meitheal expands portfolio with three biosimilars through exclusive US licensing agreement
EMS proposes merger with Hypera to form Brazil's largest drugmaker
Bio-Thera and Gedeon Richter partner to commercialize Stelara biosimilar BAT2206
Advances for Biocon Biologics’ Stelara and Eylea biosimilars
Comments (0)
Post your comment