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 use only"
Registration Number : 220MF10015
Registrant's Address : 575-1 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2008-01-09
Latest Date of Registration : 2008-01-09
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
Japanese Pharmacopoeia L-cysteine (for manufacturing purposes 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
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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 FEMA No. 3263 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FEMA No. 3263, including repackagers and relabelers. The FDA regulates FEMA No. 3263 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FEMA No. 3263 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 FEMA No. 3263 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A FEMA No. 3263 supplier is an individual or a company that provides FEMA No. 3263 active pharmaceutical ingredient (API) or FEMA No. 3263 finished formulations upon request. The FEMA No. 3263 suppliers may include FEMA No. 3263 API manufacturers, exporters, distributors and traders.
click here to find a list of FEMA No. 3263 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 FEMA No. 3263 Drug Master File in Japan (FEMA No. 3263 JDMF) empowers FEMA No. 3263 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 FEMA No. 3263 JDMF during the approval evaluation for pharmaceutical products. At the time of FEMA No. 3263 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 FEMA No. 3263 suppliers with JDMF on PharmaCompass.
We have 2 companies offering FEMA No. 3263
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