01 1Hamari PFST Co., Ltd.
02 1Kongo Chemical Co., Ltd.
01 1Benfotiamine "Yonezawa"
02 1Benfotiamine (production only)
01 2Japan
Benfotiamine (for manufacturing purposes only)
Registration Number : 217MF11200
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2007-05-15
Registration Number : 217MF10852
Registrant's Address : 1-19-40 Minamiko-Kita, Suminoe-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2007-04-27
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Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benfotiamine manufacturer or Benfotiamine supplier.
A Neurostop manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neurostop, including repackagers and relabelers. The FDA regulates Neurostop manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neurostop 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 Neurostop manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Neurostop supplier is an individual or a company that provides Neurostop active pharmaceutical ingredient (API) or Neurostop finished formulations upon request. The Neurostop suppliers may include Neurostop API manufacturers, exporters, distributors and traders.
click here to find a list of Neurostop suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Neurostop Drug Master File in Japan (Neurostop JDMF) empowers Neurostop 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 Neurostop JDMF during the approval evaluation for pharmaceutical products. At the time of Neurostop 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 Neurostop suppliers with JDMF on PharmaCompass.
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