01 2Kao Corporation
01 1SANISOL C
02 1SANISOL L-80
01 2Japan
Registration Number : 217MF10004
Registrant's Address : 1-14-10 Nihonbashi Kayabacho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-18
Latest Date of Registration : 2007-07-02
Registration Number : 217MF10005
Registrant's Address : 1-14-10 Nihonbashi Kayabacho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-18
Latest Date of Registration : 2021-10-21
A Cetalkonium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetalkonium Chloride, including repackagers and relabelers. The FDA regulates Cetalkonium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetalkonium Chloride 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 Cetalkonium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cetalkonium Chloride supplier is an individual or a company that provides Cetalkonium Chloride active pharmaceutical ingredient (API) or Cetalkonium Chloride finished formulations upon request. The Cetalkonium Chloride suppliers may include Cetalkonium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cetalkonium Chloride 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 Cetalkonium Chloride Drug Master File in Japan (Cetalkonium Chloride JDMF) empowers Cetalkonium Chloride 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 Cetalkonium Chloride JDMF during the approval evaluation for pharmaceutical products. At the time of Cetalkonium Chloride 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 Cetalkonium Chloride suppliers with JDMF on PharmaCompass.
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