01 1Alembic Pharmaceuticals Limited
02 1Corden Pharma Cheno(＾)ve SAS
03 1Jiangsu Nhwa Pharmaceutical Co. , Ltd.
01 2Fenofibrate
02 1fenofibrate
01 1China
02 1Germany
03 1India
Registration Number : 228MF10151
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2016-08-08
Latest Date of Registration : 2020-12-15
Registration Number : 222MF10028
Registrant's Address : 47, rue de Longvic B. P. 50 21301 CHENO(^)VE CEDEX FRANCE
Initial Date of Registration : 2010-01-26
Latest Date of Registration : 2010-01-26
Registration Number : 303MF10071
Registrant's Address : No. 18, Yangshan Road, Economic Development Zone, Xuzhou, Jiangsu, China.
Initial Date of Registration : 2021-04-22
Latest Date of Registration : 2021-04-22
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PharmaCompass offers a list of Fenofibrate 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 Fenofibrate manufacturer or Fenofibrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fenofibrate manufacturer or Fenofibrate supplier.
PharmaCompass also assists you with knowing the Fenofibrate API Price utilized in the formulation of products. Fenofibrate API Price is not always fixed or binding as the Fenofibrate Price is obtained through a variety of data sources. The Fenofibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fenomax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenomax, including repackagers and relabelers. The FDA regulates Fenomax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenomax 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 Fenomax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenomax supplier is an individual or a company that provides Fenomax active pharmaceutical ingredient (API) or Fenomax finished formulations upon request. The Fenomax suppliers may include Fenomax API manufacturers, exporters, distributors and traders.
click here to find a list of Fenomax 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 Fenomax Drug Master File in Japan (Fenomax JDMF) empowers Fenomax 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 Fenomax JDMF during the approval evaluation for pharmaceutical products. At the time of Fenomax 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 Fenomax suppliers with JDMF on PharmaCompass.
We have 3 companies offering Fenomax
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