01 2Permakem Asia Co., Ltd.
01 2Bethanechol chloride
01 2Japan
Registration Number : 224MF10220
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2012-11-19
Latest Date of Registration : 2012-11-19
Registration Number : 217MF10710
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2009-08-07
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PharmaCompass offers a list of Bethanechol 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 Bethanechol manufacturer or Bethanechol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bethanechol manufacturer or Bethanechol supplier.
PharmaCompass also assists you with knowing the Bethanechol API Price utilized in the formulation of products. Bethanechol API Price is not always fixed or binding as the Bethanechol Price is obtained through a variety of data sources. The Bethanechol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Myocholine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Myocholine, including repackagers and relabelers. The FDA regulates Myocholine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Myocholine 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 Myocholine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Myocholine supplier is an individual or a company that provides Myocholine active pharmaceutical ingredient (API) or Myocholine finished formulations upon request. The Myocholine suppliers may include Myocholine API manufacturers, exporters, distributors and traders.
click here to find a list of Myocholine 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 Myocholine Drug Master File in Japan (Myocholine JDMF) empowers Myocholine 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 Myocholine JDMF during the approval evaluation for pharmaceutical products. At the time of Myocholine 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 Myocholine suppliers with JDMF on PharmaCompass.
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