01 2Permachem 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 Myo Hermes manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Myo Hermes, including repackagers and relabelers. The FDA regulates Myo Hermes manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Myo Hermes 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 Myo Hermes manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Myo Hermes supplier is an individual or a company that provides Myo Hermes active pharmaceutical ingredient (API) or Myo Hermes finished formulations upon request. The Myo Hermes suppliers may include Myo Hermes API manufacturers, exporters, distributors and traders.
click here to find a list of Myo Hermes 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 Myo Hermes Drug Master File in Japan (Myo Hermes JDMF) empowers Myo Hermes 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 Myo Hermes JDMF during the approval evaluation for pharmaceutical products. At the time of Myo Hermes 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 Myo Hermes suppliers with JDMF on PharmaCompass.
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