01 1Olon S. p. A.
02 3Sumitomo Chemical Co., Ltd.
01 1Bezafibrate "KOA"
02 1Bezafibrate (OK)
03 2Japanese Pharmacopoeia bezafibrate
01 1Italy
02 3Japan
Registration Number : 218MF10019
Registrant's Address : Strada Rivoltana, km 6/7, 20053 Rodano (MI), Italy
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2021-08-16
Registration Number : 223MF10164
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2011-11-28
Latest Date of Registration : 2011-11-28
Japanese Pharmacopoeia Bezafibrate
Registration Number : 222MF10051
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2010-02-12
Latest Date of Registration : 2010-02-12
Japanese Pharmacopoeia Bezafibrate
Registration Number : 219MF10226
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2007-07-06
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PharmaCompass offers a list of Bezafibrate 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 Bezafibrate manufacturer or Bezafibrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bezafibrate manufacturer or Bezafibrate supplier.
PharmaCompass also assists you with knowing the Bezafibrate API Price utilized in the formulation of products. Bezafibrate API Price is not always fixed or binding as the Bezafibrate Price is obtained through a variety of data sources. The Bezafibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bezafibrat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bezafibrat, including repackagers and relabelers. The FDA regulates Bezafibrat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bezafibrat 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 Bezafibrat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bezafibrat supplier is an individual or a company that provides Bezafibrat active pharmaceutical ingredient (API) or Bezafibrat finished formulations upon request. The Bezafibrat suppliers may include Bezafibrat API manufacturers, exporters, distributors and traders.
click here to find a list of Bezafibrat 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 Bezafibrat Drug Master File in Japan (Bezafibrat JDMF) empowers Bezafibrat 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 Bezafibrat JDMF during the approval evaluation for pharmaceutical products. At the time of Bezafibrat 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 Bezafibrat suppliers with JDMF on PharmaCompass.
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