01 1Kobe Natural Products Chemical Co., Ltd.
02 1Permakem Asia Co., Ltd.
01 1Bromide distigmine
02 1Distigmine bromide
01 2Japan
Registration Number : 226MF10223
Registrant's Address : 3-2-34 Takatsukadai, Nishi-ku, Kobe City, Hyogo Prefecture
Initial Date of Registration : 2014-12-08
Latest Date of Registration : 2017-04-25
Registration Number : 217MF10705
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2008-10-10
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PharmaCompass offers a list of Distigmine Bromide 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 Distigmine Bromide manufacturer or Distigmine Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Distigmine Bromide manufacturer or Distigmine Bromide supplier.
PharmaCompass also assists you with knowing the Distigmine Bromide API Price utilized in the formulation of products. Distigmine Bromide API Price is not always fixed or binding as the Distigmine Bromide Price is obtained through a variety of data sources. The Distigmine Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ubretid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ubretid, including repackagers and relabelers. The FDA regulates Ubretid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ubretid 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 Ubretid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ubretid supplier is an individual or a company that provides Ubretid active pharmaceutical ingredient (API) or Ubretid finished formulations upon request. The Ubretid suppliers may include Ubretid API manufacturers, exporters, distributors and traders.
click here to find a list of Ubretid 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 Ubretid Drug Master File in Japan (Ubretid JDMF) empowers Ubretid 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 Ubretid JDMF during the approval evaluation for pharmaceutical products. At the time of Ubretid 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 Ubretid suppliers with JDMF on PharmaCompass.
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