01 1Nippon Protein Co., Ltd.
02 3Taenaka Mining Co., Ltd.
01 1Cysteine [F]
02 1Cysteine [etch]
03 1Japanese Pharmacopoeia L- cysteine
04 1Japanese Pharmacopoeia L- cysteine (production only)
01 4Japan
Japanese Pharmacopoeia L-Cysteine "For manufacturing purposes only"
Registration Number : 220MF10015
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2008-01-09
Latest Date of Registration : 2008-01-09
Japanese Pharmacopoeia L-Cysteine (for manufacturing only)
Registration Number : 220MF10209
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2008-09-29
Latest Date of Registration : 2008-09-29
Registration Number : 217MF10280
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2005-06-20
Latest Date of Registration : 2006-05-18
Registration Number : 217MF10281
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2005-06-20
Latest Date of Registration : 2006-12-08
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PharmaCompass offers a list of L-Cysteine 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 L-Cysteine manufacturer or L-Cysteine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Cysteine manufacturer or L-Cysteine supplier.
PharmaCompass also assists you with knowing the L-Cysteine API Price utilized in the formulation of products. L-Cysteine API Price is not always fixed or binding as the L-Cysteine Price is obtained through a variety of data sources. The L-Cysteine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cysteinum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cysteinum, including repackagers and relabelers. The FDA regulates Cysteinum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cysteinum 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 Cysteinum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cysteinum supplier is an individual or a company that provides Cysteinum active pharmaceutical ingredient (API) or Cysteinum finished formulations upon request. The Cysteinum suppliers may include Cysteinum API manufacturers, exporters, distributors and traders.
click here to find a list of Cysteinum 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 Cysteinum Drug Master File in Japan (Cysteinum JDMF) empowers Cysteinum 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 Cysteinum JDMF during the approval evaluation for pharmaceutical products. At the time of Cysteinum 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 Cysteinum suppliers with JDMF on PharmaCompass.
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