Registration Number : 217MF10889
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-11-07
Latest Date of Registration : 2008-03-14
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PharmaCompass offers a list of Furazolidone 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 Furazolidone manufacturer or Furazolidone supplier for your needs.
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A Furoxon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Furoxon, including repackagers and relabelers. The FDA regulates Furoxon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Furoxon 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 Furoxon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Furoxon supplier is an individual or a company that provides Furoxon active pharmaceutical ingredient (API) or Furoxon finished formulations upon request. The Furoxon suppliers may include Furoxon API manufacturers, exporters, distributors and traders.
click here to find a list of Furoxon 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 Furoxon Drug Master File in Japan (Furoxon JDMF) empowers Furoxon 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 Furoxon JDMF during the approval evaluation for pharmaceutical products. At the time of Furoxon 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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