Eisai America, Inc.
Eisai Inc. (U.S.A.) Alias
1941-12-06
Japan
Research and development of pharmaceuticals
Manufacture of pharmaceuticals
Sale of pharmaceuticals
Import and export of pharmaceuticals
Pharmaceutical development and marketing
Research and development of drugs
Manufacturing of pharmaceutical products
Corporate venture capital
4-6-10 Koishikawa, Bunkyo-ku, Tokyo 112-8088, Japan
Haruo Naito
44,986 JPY
2,998 people
10,917 people

43 entries
DateDescription
1950 Nihon Eisai Co., Ltd.'s contraceptive suppository : Sampoon : , researched and developed during Japan's postwar baby boom, receives official approval from the Japanese government.
1950 Nihon Eisai Co., Ltd. launches cardiotonic : Neophyllin : in Japan.
1952 Nihon Eisai Co., Ltd. launches high-dosage vitamin B1 and B2 product : Chocola BB Tablets : in Japan.
1952 Nihon Eisai Co., Ltd. launches motion sickness remedy : Travelmin : in Japan.
1955 The company changes its name from Nihon Eisai Co., Ltd. to Eisai Co., Ltd., as it is known today.
1957 Eisai rolls out its first three-year mid-term plan.
1957 Eisai's Head Office building is completed in Tokyo.
1961 Eisai opens its Taipei Office (now part of Eisai Taiwan Inc.), the company's first overseas branch, in Taiwan.
1961 Eisai is publicly listed in the First Section of both the Tokyo and Osaka Stock Exchanges.
1961 Gastrointestinal remedies : Saclon : and : Saclon Tablets : , recognizable for their distinct green hue even today, are launched in Japan.
1964 Toyoji Naito receives the Japan Marketing Award, which recognizes people who have made a significant contribution to marketing and advertising in Japan.
1966 The Kawashima Plant is completed in Gifu, central Japan.
1966 Kawashima Plant opening ceremony.
1966 Founder Toyoji Naito is appointed as chairman and Yuji Naito as company president.
1966 A three-tier representative director system is introduced: Chairman Toyoji Naito, President Yuji Naito, and Executive Vice President Tatsuo Naito.
1969 Youda Co., Ltd. is established as a pharmaceutical imports subsidiary in Taiwan.
1970 PT Eisai Indonesia is established as a pharmaceutical manufacturing and sales subsidiary in Indonesia.
1970 Toyoji Naito resigns as representative director and chairman to assume director and honorary chairman roles.
1971 Toyoji opens the Naito Museum of Pharmaceutical Science and Industry, Japan's first pharmaceutical museum, in Gifu.
1974 Eisai (Malaysia) Sdn. Bhd. and Hi-Eisai Pharmaceutical Inc. are established as pharmaceutical sales subsidiaries in Malaysia and the Philippines, respectively.
1974 Metabolic cardiotonic : Neuquinon : is launched in Japan.
1977 Naturally derived vitamin E product : Juvelux : is launched in Japan.
1978 Eisai's founder Toyoji Naito passes away at age 89.
1978 Peripheral neuropathy treatment : Methycobal : is launched in Japan.
1979 Eisai Asia Regional Services Pte. Ltd. is established as a sales support and management services subsidiary in Singapore.
1988 Eisai America, Inc. is established as a clinical research subsidiary in New Jersey, the United States.
1997 Eisai Inc. North Carolina Plant is established as a pharmaceutical manufacturing and formulation R&D facility at Research Triangle Park in North Carolina, the United States.
1997 Anti-Alzheimer's agent : Aricept : is launched in the United States, the United Kingdom and Germany.
1999 Pariet : is launched under the brand name : AcipHex : in the United States.
2002 Eisai Medical Research Inc. is established as a clinical research subsidiary in New Jersey, the United States.
2006 Eisai acquires four anticancer agents from Ligand Pharmaceuticals Inc. in the United States.
2007 Eisai acquires Morphotek Inc., a bioventure specialized in antibody research, in the United States.
2008 Eisai acquires MGI Pharma Inc., an oncology biopharmaceutical company in the United States.
2010 Halaven is launched in the United States.
2010 H3 Biomedicine Inc. is established as a research subsidiary in the United States.
2014 Fycompa is launched in the United States.
2015 Lenvima is launched in the United States, Japan and Europe.
2017 Collaboration agreement with Biogen to develop and commercialize investigational Alzheimer's disease treatments including aducanumab expanded.
2018 Eisai agrees upon a strategic collaboration for Lenvima with Merck & Co., Inc., Kenilworth, N.J., U.S.A.
2019 Eisai Center for Genetics Guided Dementia Discovery (G2D2) in Massachusetts, U.S., commences full-scale operation.
2020 DAYVIGO (insomnia treatment) is launched in the United States and Japan.
2023 Alzheimer’s disease treatment LEQEMBI is granted accelerated approval and launched in the United States.
2023 LEQEMBI is granted traditional approval by the FDA.
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2026-09-21 18:10 (Model: ggml-org/gpt-oss-20b )
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