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 L-Cystin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Cystin, including repackagers and relabelers. The FDA regulates L-Cystin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Cystin 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 L-Cystin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L-Cystin supplier is an individual or a company that provides L-Cystin active pharmaceutical ingredient (API) or L-Cystin finished formulations upon request. The L-Cystin suppliers may include L-Cystin API manufacturers, exporters, distributors and traders.
click here to find a list of L-Cystin 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 L-Cystin Drug Master File in Japan (L-Cystin JDMF) empowers L-Cystin 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 L-Cystin JDMF during the approval evaluation for pharmaceutical products. At the time of L-Cystin 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 L-Cystin suppliers with JDMF on PharmaCompass.
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