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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PharmaCompass also assists you with knowing the Colistimethate Sodium API Price utilized in the formulation of products. Colistimethate Sodium API Price is not always fixed or binding as the Colistimethate Sodium Price is obtained through a variety of data sources. The Colistimethate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Coly-Mycin M Parenteral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Coly-Mycin M Parenteral, including repackagers and relabelers. The FDA regulates Coly-Mycin M Parenteral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Coly-Mycin M Parenteral 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 Coly-Mycin M Parenteral supplier is an individual or a company that provides Coly-Mycin M Parenteral active pharmaceutical ingredient (API) or Coly-Mycin M Parenteral finished formulations upon request. The Coly-Mycin M Parenteral suppliers may include Coly-Mycin M Parenteral API manufacturers, exporters, distributors and traders.
click here to find a list of Coly-Mycin M Parenteral 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 Coly-Mycin M Parenteral Drug Master File in Japan (Coly-Mycin M Parenteral JDMF) empowers Coly-Mycin M Parenteral 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 Coly-Mycin M Parenteral JDMF during the approval evaluation for pharmaceutical products. At the time of Coly-Mycin M Parenteral 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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