01 1Sekisui Medical Co., Ltd.
01 1Clemastine fumarate
01 1Japan
Registration Number : 219MF10016
Registrant's Address : 3-13-5 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2007-01-18
Latest Date of Registration : 2007-01-18
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PharmaCompass offers a list of Clemastine 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 Clemastine manufacturer or Clemastine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clemastine manufacturer or Clemastine supplier.
PharmaCompass also assists you with knowing the Clemastine API Price utilized in the formulation of products. Clemastine API Price is not always fixed or binding as the Clemastine Price is obtained through a variety of data sources. The Clemastine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tavegil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tavegil, including repackagers and relabelers. The FDA regulates Tavegil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tavegil 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 Tavegil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tavegil supplier is an individual or a company that provides Tavegil active pharmaceutical ingredient (API) or Tavegil finished formulations upon request. The Tavegil suppliers may include Tavegil API manufacturers, exporters, distributors and traders.
click here to find a list of Tavegil 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 Tavegil Drug Master File in Japan (Tavegil JDMF) empowers Tavegil 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 Tavegil JDMF during the approval evaluation for pharmaceutical products. At the time of Tavegil 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 Tavegil suppliers with JDMF on PharmaCompass.
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