01 1AMINO GmbH
02 2Ajinomoto Health & Nutrition North America, Inc.
03 1Kyowa Hakko Bio Co., Ltd.
01 3Japanese Pharmacopoeia L- tryptophan (production only)
02 1L-tryptophan
01 1Germany
02 3Japan
Japanese Pharmacopoeia L-Tryptophan (for manufacturing only)
Registration Number : 227MF10115
Registrant's Address : 4020 Ajinomoto Drive Raleigh, North Carolina 27610, USA
Initial Date of Registration : 2015-04-21
Latest Date of Registration : 2015-04-21
Japanese Pharmacopoeia L-Tryptophan (for manufacturing only)
Registration Number : 220MF10074
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
Registration Number : 306MF10053
Registrant's Address : An der Zucker-Raffinerie 9, 38373 Frellstedt, Germany
Initial Date of Registration : 2024-04-10
Latest Date of Registration : 2024-04-10
Japanese Pharmacopoeia L-Tryptophan (for manufacturing only)
Registration Number : 217MF10228
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2006-11-15
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PharmaCompass offers a list of Tryptophan API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tryptophan manufacturer or Tryptophan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tryptophan manufacturer or Tryptophan supplier.
PharmaCompass also assists you with knowing the Tryptophan API Price utilized in the formulation of products. Tryptophan API Price is not always fixed or binding as the Tryptophan Price is obtained through a variety of data sources. The Tryptophan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tryptophan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tryptophan, including repackagers and relabelers. The FDA regulates Tryptophan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tryptophan 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 Tryptophan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tryptophan supplier is an individual or a company that provides Tryptophan active pharmaceutical ingredient (API) or Tryptophan finished formulations upon request. The Tryptophan suppliers may include Tryptophan API manufacturers, exporters, distributors and traders.
click here to find a list of Tryptophan 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 Tryptophan Drug Master File in Japan (Tryptophan JDMF) empowers Tryptophan 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 Tryptophan JDMF during the approval evaluation for pharmaceutical products. At the time of Tryptophan 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 Tryptophan suppliers with JDMF on PharmaCompass.
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