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.
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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 Propifenazona manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propifenazona, including repackagers and relabelers. The FDA regulates Propifenazona manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propifenazona API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Propifenazona supplier is an individual or a company that provides Propifenazona active pharmaceutical ingredient (API) or Propifenazona finished formulations upon request. The Propifenazona suppliers may include Propifenazona API manufacturers, exporters, distributors and traders.
click here to find a list of Propifenazona 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 Propifenazona Drug Master File in Japan (Propifenazona JDMF) empowers Propifenazona 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 Propifenazona JDMF during the approval evaluation for pharmaceutical products. At the time of Propifenazona 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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