01 1Kyowa Hakko Bio Co., Ltd.
01 1Japanese Pharmacopoeia citicoline (production only)
01 1Japan
Japanese Pharmacopoeia Citicoline (for manufacturing only)
Registration Number : 217MF10245
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2017-04-14
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PharmaCompass offers a list of Citicoline Sodium 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 Citicoline Sodium manufacturer or Citicoline Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Citicoline Sodium manufacturer or Citicoline Sodium supplier.
PharmaCompass also assists you with knowing the Citicoline Sodium API Price utilized in the formulation of products. Citicoline Sodium API Price is not always fixed or binding as the Citicoline Sodium Price is obtained through a variety of data sources. The Citicoline Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CDP-cholin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CDP-cholin, including repackagers and relabelers. The FDA regulates CDP-cholin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CDP-cholin 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 CDP-cholin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CDP-cholin supplier is an individual or a company that provides CDP-cholin active pharmaceutical ingredient (API) or CDP-cholin finished formulations upon request. The CDP-cholin suppliers may include CDP-cholin API manufacturers, exporters, distributors and traders.
click here to find a list of CDP-cholin 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 CDP-cholin Drug Master File in Japan (CDP-cholin JDMF) empowers CDP-cholin 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 CDP-cholin JDMF during the approval evaluation for pharmaceutical products. At the time of CDP-cholin 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 CDP-cholin suppliers with JDMF on PharmaCompass.
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