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
A Propyphenazone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propyphenazone, including repackagers and relabelers. The FDA regulates Propyphenazone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propyphenazone 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 Propyphenazone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Propyphenazone supplier is an individual or a company that provides Propyphenazone active pharmaceutical ingredient (API) or Propyphenazone finished formulations upon request. The Propyphenazone suppliers may include Propyphenazone API manufacturers, exporters, distributors and traders.
click here to find a list of Propyphenazone 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 Propyphenazone Drug Master File in Japan (Propyphenazone JDMF) empowers Propyphenazone 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 Propyphenazone JDMF during the approval evaluation for pharmaceutical products. At the time of Propyphenazone 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 Propyphenazone suppliers with JDMF on PharmaCompass.
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