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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PharmaCompass offers a list of Benfotiamine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Benfotiamine manufacturer or Benfotiamine supplier for your needs.
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A Benfotiamina [INN-Spanish] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benfotiamina [INN-Spanish], including repackagers and relabelers. The FDA regulates Benfotiamina [INN-Spanish] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benfotiamina [INN-Spanish] 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 Benfotiamina [INN-Spanish] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Benfotiamina [INN-Spanish] supplier is an individual or a company that provides Benfotiamina [INN-Spanish] active pharmaceutical ingredient (API) or Benfotiamina [INN-Spanish] finished formulations upon request. The Benfotiamina [INN-Spanish] suppliers may include Benfotiamina [INN-Spanish] API manufacturers, exporters, distributors and traders.
click here to find a list of Benfotiamina [INN-Spanish] 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 Benfotiamina [INN-Spanish] Drug Master File in Japan (Benfotiamina [INN-Spanish] JDMF) empowers Benfotiamina [INN-Spanish] 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 Benfotiamina [INN-Spanish] JDMF during the approval evaluation for pharmaceutical products. At the time of Benfotiamina [INN-Spanish] 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 Benfotiamina [INN-Spanish] suppliers with JDMF on PharmaCompass.
We have 2 companies offering Benfotiamina [INN-Spanish]
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