01 1Daiichi Sankyo Co., Ltd.
02 1Takeda Pharmaceutical Company Limited
01 1Day stations dihydrocodeine phosphate (production only)
02 1Dihydrocodeine phosphate "Takeda"
01 2Japan
Japanese Pharmacopoeia Dihydrocodeine Phosphate (for manufacturing only)
Registration Number : 218MF11021
Registrant's Address : 3-5-1 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2009-04-08
Dihydrocodeine phosphate "Takeda"
Registration Number : 219MF10064
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 4-1-1
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2019-07-26
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PharmaCompass offers a list of Codeine Phosphate 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 Codeine Phosphate manufacturer or Codeine Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Codeine Phosphate manufacturer or Codeine Phosphate supplier.
PharmaCompass also assists you with knowing the Codeine Phosphate API Price utilized in the formulation of products. Codeine Phosphate API Price is not always fixed or binding as the Codeine Phosphate Price is obtained through a variety of data sources. The Codeine Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PROMETH VC W/ CODEINE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PROMETH VC W/ CODEINE, including repackagers and relabelers. The FDA regulates PROMETH VC W/ CODEINE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PROMETH VC W/ CODEINE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A PROMETH VC W/ CODEINE supplier is an individual or a company that provides PROMETH VC W/ CODEINE active pharmaceutical ingredient (API) or PROMETH VC W/ CODEINE finished formulations upon request. The PROMETH VC W/ CODEINE suppliers may include PROMETH VC W/ CODEINE API manufacturers, exporters, distributors and traders.
click here to find a list of PROMETH VC W/ CODEINE 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 PROMETH VC W/ CODEINE Drug Master File in Japan (PROMETH VC W/ CODEINE JDMF) empowers PROMETH VC W/ CODEINE 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 PROMETH VC W/ CODEINE JDMF during the approval evaluation for pharmaceutical products. At the time of PROMETH VC W/ CODEINE JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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