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 purposes 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 : 1-1 Doshomachi 4-chome, Chuo-ku, Osaka City, Osaka Prefecture
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 Codeine Phosphate Hemihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Codeine Phosphate Hemihydrate, including repackagers and relabelers. The FDA regulates Codeine Phosphate Hemihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Codeine Phosphate Hemihydrate 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 Codeine Phosphate Hemihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Codeine Phosphate Hemihydrate supplier is an individual or a company that provides Codeine Phosphate Hemihydrate active pharmaceutical ingredient (API) or Codeine Phosphate Hemihydrate finished formulations upon request. The Codeine Phosphate Hemihydrate suppliers may include Codeine Phosphate Hemihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Codeine Phosphate Hemihydrate 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 Codeine Phosphate Hemihydrate Drug Master File in Japan (Codeine Phosphate Hemihydrate JDMF) empowers Codeine Phosphate Hemihydrate 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 Codeine Phosphate Hemihydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Codeine Phosphate Hemihydrate 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 Codeine Phosphate Hemihydrate suppliers with JDMF on PharmaCompass.
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