01 1Everlight Chemical Industrial Corporation
01 1Felodipine
01 1Taiwan
Registration Number : 219MF10301
Registrant's Address : 6Floor, Chung Ting Building No. 77, Section 2, Tun Hua South Road, Taipei, Taiwan
Initial Date of Registration : 2007-09-18
Latest Date of Registration : 2023-03-23
A Felodipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Felodipine, including repackagers and relabelers. The FDA regulates Felodipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Felodipine 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 Felodipine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Felodipine supplier is an individual or a company that provides Felodipine active pharmaceutical ingredient (API) or Felodipine finished formulations upon request. The Felodipine suppliers may include Felodipine API manufacturers, exporters, distributors and traders.
click here to find a list of Felodipine 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 Felodipine Drug Master File in Japan (Felodipine JDMF) empowers Felodipine 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 Felodipine JDMF during the approval evaluation for pharmaceutical products. At the time of Felodipine 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 Felodipine suppliers with JDMF on PharmaCompass.
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