Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 2Evonik Rexim S. A. S.
02 1Ajinomoto Health & Nutrition North America, Inc.
03 2Kyowa Hakko Bio Co., Ltd.
04 1Shanghai Ajinomoto Amino Acid Co., Ltd.
01 4Japanese Pharmacopoeia L- threonine (production only)
02 2L- threonine L-Threonine
01 2Germany
02 4Japan
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 218MF10965
Registrant's Address : 33, Rue de Verdun Ham, France
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2019-07-19
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 218MF10659
Registrant's Address : 33, Rue de Verdun Ham France
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2006-07-24
Japanese Pharmacopoeia L-Threonine (for manufacturing only)
Registration Number : 218MF10907
Registrant's Address : No. 718, Rongle East Road, Songjiang District, Shanghai, People's Republic of China
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
Japanese Pharmacopoeia L-Threonine (for manufacturing only)
Registration Number : 220MF10073
Registrant's Address : 4020 Ajinomoto Drive Raleigh, North Carolina 27610, USA
Initial Date of Registration : 2008-03-14
Latest Date of Registration : 2008-03-14
Japanese Pharmacopoeia L-Threonine (for manufacturing only)
Registration Number : 226MF10004
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2014-01-08
Latest Date of Registration : 2014-01-08
Japanese Pharmacopoeia L-Threonine (for manufacturing only)
Registration Number : 217MF10229
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2006-11-15
A Threonine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Threonine, including repackagers and relabelers. The FDA regulates Threonine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Threonine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Threonine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Threonine supplier is an individual or a company that provides Threonine active pharmaceutical ingredient (API) or Threonine finished formulations upon request. The Threonine suppliers may include Threonine API manufacturers, exporters, distributors and traders.
click here to find a list of Threonine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Threonine Drug Master File in Japan (Threonine JDMF) empowers Threonine API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Threonine JDMF during the approval evaluation for pharmaceutical products. At the time of Threonine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Threonine suppliers with JDMF on PharmaCompass.
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