01 1Daito Co., Ltd.
02 1Permakem Asia Co., Ltd.
03 1Shiratori Pharmaceutical Co., Ltd.
01 1Emme Das Chin fumarate
02 1Fumaric acid emedastine
03 1Japanese Pharmacopoeia fumaric acid emedastin production dedicated
01 3Japan
Registration Number : 228MF10218
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2016-11-15
Latest Date of Registration : 2017-10-03
Registration Number : 217MF11139
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2008-09-19
Japanese Pharmacopoeia Emedastine Fumarate For manufacturing only
Registration Number : 230MF10017
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2018-02-05
Latest Date of Registration : 2018-02-05
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PharmaCompass offers a list of Emedastine Fumarate 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 Emedastine Fumarate manufacturer or Emedastine Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Emedastine Fumarate manufacturer or Emedastine Fumarate supplier.
PharmaCompass also assists you with knowing the Emedastine Fumarate API Price utilized in the formulation of products. Emedastine Fumarate API Price is not always fixed or binding as the Emedastine Fumarate Price is obtained through a variety of data sources. The Emedastine Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Emedastine Difumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emedastine Difumarate, including repackagers and relabelers. The FDA regulates Emedastine Difumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emedastine Difumarate 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 Emedastine Difumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Emedastine Difumarate supplier is an individual or a company that provides Emedastine Difumarate active pharmaceutical ingredient (API) or Emedastine Difumarate finished formulations upon request. The Emedastine Difumarate suppliers may include Emedastine Difumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Emedastine Difumarate 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 Emedastine Difumarate Drug Master File in Japan (Emedastine Difumarate JDMF) empowers Emedastine Difumarate 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 Emedastine Difumarate JDMF during the approval evaluation for pharmaceutical products. At the time of Emedastine Difumarate 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 Emedastine Difumarate suppliers with JDMF on PharmaCompass.
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