01 1Hebei Shengxue Dacheng Pharmaceutical Co. , Ltd.
02 1Sun Pharma Manufacturing Co., Ltd.
03 2Xellia Pharmaceuticals ApS
01 1Colistin Sodium Methanesulfonate
02 1Colistin methanesulfonate sodium sterile
03 1Colistin sodium methanesulfonate
04 1Colistin sodium methanesulfonate (prepared only)
01 1China
02 2Denmark
03 1Japan
Colistin Sodium Methanesulfonate
Registration Number : 303MF10108
Registrant's Address : No. 50 Shengxue Road, Luncheng Shijiazhuang, Hebei Province, China
Initial Date of Registration : 2021-07-16
Latest Date of Registration : 2021-07-16
Colistin Sodium Methanesulfonate (for manufacturing purposes only)
Registration Number : 217MF10573
Registrant's Address : 1130-4 Kamekubo, Fujimino City, Saitama Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2008-11-10
Colistin Sodium Methanesulfonate Sterile
Registration Number : 223MF10046
Registrant's Address : Dalslandsgade 11, DK-2300 Copenhagen-S, Denmark
Initial Date of Registration : 2011-03-25
Latest Date of Registration : 2011-03-25
Colistin Sodium Methanesulfonate
Registration Number : 221MF10198
Registrant's Address : Dalslandsgade 11, DK-2300 Copenhagen-S, Denmark
Initial Date of Registration : 2009-09-14
Latest Date of Registration : 2023-10-04
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PharmaCompass offers a list of Colistimethate Sodium 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 Colistimethate Sodium manufacturer or Colistimethate Sodium supplier for your needs.
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A Colistimethate sodium methanesulfonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Colistimethate sodium methanesulfonate, including repackagers and relabelers. The FDA regulates Colistimethate sodium methanesulfonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Colistimethate sodium methanesulfonate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Colistimethate sodium methanesulfonate supplier is an individual or a company that provides Colistimethate sodium methanesulfonate active pharmaceutical ingredient (API) or Colistimethate sodium methanesulfonate finished formulations upon request. The Colistimethate sodium methanesulfonate suppliers may include Colistimethate sodium methanesulfonate API manufacturers, exporters, distributors and traders.
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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 Colistimethate sodium methanesulfonate Drug Master File in Japan (Colistimethate sodium methanesulfonate JDMF) empowers Colistimethate sodium methanesulfonate 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 Colistimethate sodium methanesulfonate JDMF during the approval evaluation for pharmaceutical products. At the time of Colistimethate sodium methanesulfonate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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