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.
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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 amezinium metisulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of amezinium metisulfate, including repackagers and relabelers. The FDA regulates amezinium metisulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. amezinium metisulfate 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 amezinium metisulfate supplier is an individual or a company that provides amezinium metisulfate active pharmaceutical ingredient (API) or amezinium metisulfate finished formulations upon request. The amezinium metisulfate suppliers may include amezinium metisulfate API manufacturers, exporters, distributors and traders.
click here to find a list of amezinium metisulfate 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 amezinium metisulfate Drug Master File in Japan (amezinium metisulfate JDMF) empowers amezinium metisulfate 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 amezinium metisulfate JDMF during the approval evaluation for pharmaceutical products. At the time of amezinium metisulfate 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 amezinium metisulfate suppliers with JDMF on PharmaCompass.
We have 2 companies offering amezinium metisulfate
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