01 2NOF Corporation
01 1Nissan cation F2-50E
02 1Nissan cation F2-50EN
01 2Japan
Registration Number : 222MF10038
Registrant's Address : 20-3 Ebisu 4-chome, Shibuya-ku, Tokyo
Initial Date of Registration : 2010-01-28
Latest Date of Registration : 2010-01-28
Registration Number : 217MF11161
Registrant's Address : 20-3 Ebisu 4-chome, Shibuya-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-01-28
16
PharmaCompass offers a list of Didecyl Dimethyl Ammonium Chloride 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 Didecyl Dimethyl Ammonium Chloride manufacturer or Didecyl Dimethyl Ammonium Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Didecyl Dimethyl Ammonium Chloride API Price utilized in the formulation of products. Didecyl Dimethyl Ammonium Chloride API Price is not always fixed or binding as the Didecyl Dimethyl Ammonium Chloride Price is obtained through a variety of data sources. The Didecyl Dimethyl Ammonium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DDAC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DDAC, including repackagers and relabelers. The FDA regulates DDAC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DDAC 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 DDAC supplier is an individual or a company that provides DDAC active pharmaceutical ingredient (API) or DDAC finished formulations upon request. The DDAC suppliers may include DDAC API manufacturers, exporters, distributors and traders.
click here to find a list of DDAC 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 DDAC Drug Master File in Japan (DDAC JDMF) empowers DDAC 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 DDAC JDMF during the approval evaluation for pharmaceutical products. At the time of DDAC 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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