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 LP00304 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LP00304, including repackagers and relabelers. The FDA regulates LP00304 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LP00304 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 LP00304 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LP00304 supplier is an individual or a company that provides LP00304 active pharmaceutical ingredient (API) or LP00304 finished formulations upon request. The LP00304 suppliers may include LP00304 API manufacturers, exporters, distributors and traders.
click here to find a list of LP00304 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 LP00304 Drug Master File in Japan (LP00304 JDMF) empowers LP00304 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 LP00304 JDMF during the approval evaluation for pharmaceutical products. At the time of LP00304 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 LP00304 suppliers with JDMF on PharmaCompass.
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