01 1Kongo Chemical Co., Ltd.
01 1Isopropyl antipyrine (production only)
01 1Japan
Isopropylantipyrine (for manufacturing only)
Registration Number : 217MF11189
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2013-01-31
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PharmaCompass offers a list of Propyphenazone 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 Propyphenazone manufacturer or Propyphenazone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propyphenazone manufacturer or Propyphenazone supplier.
PharmaCompass also assists you with knowing the Propyphenazone API Price utilized in the formulation of products. Propyphenazone API Price is not always fixed or binding as the Propyphenazone Price is obtained through a variety of data sources. The Propyphenazone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Demex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Demex, including repackagers and relabelers. The FDA regulates Demex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Demex 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 Demex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Demex supplier is an individual or a company that provides Demex active pharmaceutical ingredient (API) or Demex finished formulations upon request. The Demex suppliers may include Demex API manufacturers, exporters, distributors and traders.
click here to find a list of Demex 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 Demex Drug Master File in Japan (Demex JDMF) empowers Demex 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 Demex JDMF during the approval evaluation for pharmaceutical products. At the time of Demex 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 Demex suppliers with JDMF on PharmaCompass.
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