01 1Daiichi Sankyo Co., Ltd.
02 1Takeda Pharmaceutical Company Limited
01 1Codeine acid hydrate "Takeda"
02 1Day stations codeine acid hydrate (production only)
01 2Japan
Japanese Pharmacopoeia Codeine Phosphate Hydrate (For manufacturing purposes only)
Registration Number : 219MF10035
Registrant's Address : 3-5-1 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-02-13
Latest Date of Registration : 2009-04-08
Codeine phosphate hydrate "Takeda"
Registration Number : 218MF10632
Registrant's Address : 1-1 Doshomachi 4-chome, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2006-07-20
Latest Date of Registration : 2020-04-17
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PharmaCompass offers a list of Codeine 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 manufacturer or Codeine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Codeine manufacturer or Codeine supplier.
PharmaCompass also assists you with knowing the Codeine API Price utilized in the formulation of products. Codeine API Price is not always fixed or binding as the Codeine Price is obtained through a variety of data sources. The Codeine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A metilmorfina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of metilmorfina, including repackagers and relabelers. The FDA regulates metilmorfina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. metilmorfina 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 metilmorfina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A metilmorfina supplier is an individual or a company that provides metilmorfina active pharmaceutical ingredient (API) or metilmorfina finished formulations upon request. The metilmorfina suppliers may include metilmorfina API manufacturers, exporters, distributors and traders.
click here to find a list of metilmorfina 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 metilmorfina Drug Master File in Japan (metilmorfina JDMF) empowers metilmorfina 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 metilmorfina JDMF during the approval evaluation for pharmaceutical products. At the time of metilmorfina 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 metilmorfina suppliers with JDMF on PharmaCompass.
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