Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1ChemAgis Ltd.
02 1Alembic Pharmaceuticals Limited
03 1Corden Pharma Cheno(＾)ve SAS
04 1Jiangsu Nhwa Pharmaceutical Co. , Ltd.
01 3Fenofibrate
02 1fenofibrate
01 1China
02 1France
03 1Germany
04 1India
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 220MF10040
Registrant's Address : 29, Lehi St. , Bnei Brak P. O. Box 2231, Israel
Initial Date of Registration : 2008-02-05
Latest Date of Registration : 2008-02-05
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
A Fenofibrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenofibrate, including repackagers and relabelers. The FDA regulates Fenofibrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenofibrate 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 Fenofibrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenofibrate supplier is an individual or a company that provides Fenofibrate active pharmaceutical ingredient (API) or Fenofibrate finished formulations upon request. The Fenofibrate suppliers may include Fenofibrate API manufacturers, exporters, distributors and traders.
click here to find a list of Fenofibrate 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 Fenofibrate Drug Master File in Japan (Fenofibrate JDMF) empowers Fenofibrate 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 Fenofibrate JDMF during the approval evaluation for pharmaceutical products. At the time of Fenofibrate 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 Fenofibrate suppliers with JDMF on PharmaCompass.
We have 4 companies offering Fenofibrate
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