01 1Sumitomo Chemical Co., Ltd.
01 1Phenothrin
01 1Japan
Registration Number : 225MF10106
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2013-05-20
Latest Date of Registration : 2014-02-05
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PharmaCompass offers a list of Phenothrin 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 Phenothrin manufacturer or Phenothrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenothrin manufacturer or Phenothrin supplier.
PharmaCompass also assists you with knowing the Phenothrin API Price utilized in the formulation of products. Phenothrin API Price is not always fixed or binding as the Phenothrin Price is obtained through a variety of data sources. The Phenothrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fenotrina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenotrina, including repackagers and relabelers. The FDA regulates Fenotrina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenotrina API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fenotrina supplier is an individual or a company that provides Fenotrina active pharmaceutical ingredient (API) or Fenotrina finished formulations upon request. The Fenotrina suppliers may include Fenotrina API manufacturers, exporters, distributors and traders.
click here to find a list of Fenotrina 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 Fenotrina Drug Master File in Japan (Fenotrina JDMF) empowers Fenotrina 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 Fenotrina JDMF during the approval evaluation for pharmaceutical products. At the time of Fenotrina 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 Fenotrina suppliers with JDMF on PharmaCompass.
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