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
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PharmaCompass offers a list of Felodipine 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 Felodipine manufacturer or Felodipine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Felodipine manufacturer or Felodipine supplier.
PharmaCompass also assists you with knowing the Felodipine API Price utilized in the formulation of products. Felodipine API Price is not always fixed or binding as the Felodipine Price is obtained through a variety of data sources. The Felodipine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Renedil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Renedil, including repackagers and relabelers. The FDA regulates Renedil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Renedil 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 Renedil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Renedil supplier is an individual or a company that provides Renedil active pharmaceutical ingredient (API) or Renedil finished formulations upon request. The Renedil suppliers may include Renedil API manufacturers, exporters, distributors and traders.
click here to find a list of Renedil 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 Renedil Drug Master File in Japan (Renedil JDMF) empowers Renedil 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 Renedil JDMF during the approval evaluation for pharmaceutical products. At the time of Renedil 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 Renedil suppliers with JDMF on PharmaCompass.
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