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