Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Rexim (Nanning) Pharmaceutical Co. , Ltd.
02 1Evonik Rexim S. A. S.
03 1Ajinomoto Co., Inc.
04 1Kyowa Hakko Bio Co., Ltd.
05 1Shanghai Ajinomoto Amino Acid Co., Ltd.
01 3Japanese Pharmacopoeia L- phenylalanine (production only)
02 1L- phenylalanine L-Phenylalanine
03 1L-Phenylalanine L-Phenylalanine
01 2Germany
02 3Japan
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 231MF10069
Registrant's Address : No. 46 Wenjiang Road, Wuming District, Nanning, 530199, Guangxi, P. R. China
Initial Date of Registration : 2019-03-11
Latest Date of Registration : 2019-03-11
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 218MF10966
Registrant's Address : 33, Rue de Verdun Ham, France
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2012-01-16
Japanese Pharmacopoeia L-Phenylalanine (for manufacturing only)
Registration Number : 226MF10085
Registrant's Address : No. 718, Rongle East Road, Songjiang District, Shanghai, People's Republic of China
Initial Date of Registration : 2014-05-09
Latest Date of Registration : 2014-05-09
Japanese Pharmacopoeia L-Phenylalanine (for manufacturing only)
Registration Number : 217MF10376
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-07-27
Latest Date of Registration : 2008-04-11
Japanese Pharmacopoeia L-Phenylalanine (for manufacturing only)
Registration Number : 217MF10232
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2006-11-15
34
PharmaCompass offers a list of Phenylalanine 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 Phenylalanine manufacturer or Phenylalanine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenylalanine manufacturer or Phenylalanine supplier.
PharmaCompass also assists you with knowing the Phenylalanine API Price utilized in the formulation of products. Phenylalanine API Price is not always fixed or binding as the Phenylalanine Price is obtained through a variety of data sources. The Phenylalanine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A phe manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of phe, including repackagers and relabelers. The FDA regulates phe manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. phe 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 phe manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A phe supplier is an individual or a company that provides phe active pharmaceutical ingredient (API) or phe finished formulations upon request. The phe suppliers may include phe API manufacturers, exporters, distributors and traders.
click here to find a list of phe 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 phe Drug Master File in Japan (phe JDMF) empowers phe 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 phe JDMF during the approval evaluation for pharmaceutical products. At the time of phe 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 phe suppliers with JDMF on PharmaCompass.
We have 3 companies offering phe
Get in contact with the supplier of your choice:
