01 1Ohara Pharmaceutical Co., Ltd.
02 1Sanpo Chemical Industry Co., Ltd.
01 1Ameji methylsulfate sulfate (manufactured only)
02 1Methyl sulfate amezinium
01 2Japan
Amezinium methylsulfate (for manufacturing purposes only)
Registration Number : 221MF10217
Registrant's Address : 7-30-7 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2009-09-30
Latest Date of Registration : 2009-09-30
Registration Number : 217MF11219
Registrant's Address : 121-15 Torino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-10-20
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PharmaCompass offers a list of Supratonin 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 Supratonin manufacturer or Supratonin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Supratonin manufacturer or Supratonin supplier.
PharmaCompass also assists you with knowing the Supratonin API Price utilized in the formulation of products. Supratonin API Price is not always fixed or binding as the Supratonin Price is obtained through a variety of data sources. The Supratonin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Regulton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Regulton, including repackagers and relabelers. The FDA regulates Regulton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Regulton API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Regulton supplier is an individual or a company that provides Regulton active pharmaceutical ingredient (API) or Regulton finished formulations upon request. The Regulton suppliers may include Regulton API manufacturers, exporters, distributors and traders.
click here to find a list of Regulton 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 Regulton Drug Master File in Japan (Regulton JDMF) empowers Regulton 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 Regulton JDMF during the approval evaluation for pharmaceutical products. At the time of Regulton 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 Regulton suppliers with JDMF on PharmaCompass.
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