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