01 2Tokyo Chemical Industry Co., Ltd.
01 1Methyl sulfate neostigmine
02 1Neostigmine bromide
01 2Japan
Registration Number : 217MF11160
Registrant's Address : 6-15-9 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-10-20
Registration Number : 217MF11158
Registrant's Address : 6-15-9 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-10-20
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PharmaCompass offers a list of Neostigmine Methylsulfate 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 Neostigmine Methylsulfate manufacturer or Neostigmine Methylsulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Neostigmine Methylsulfate API Price utilized in the formulation of products. Neostigmine Methylsulfate API Price is not always fixed or binding as the Neostigmine Methylsulfate Price is obtained through a variety of data sources. The Neostigmine Methylsulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prozerin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prozerin, including repackagers and relabelers. The FDA regulates Prozerin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prozerin 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 Prozerin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prozerin supplier is an individual or a company that provides Prozerin active pharmaceutical ingredient (API) or Prozerin finished formulations upon request. The Prozerin suppliers may include Prozerin API manufacturers, exporters, distributors and traders.
click here to find a list of Prozerin 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 Prozerin Drug Master File in Japan (Prozerin JDMF) empowers Prozerin 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 Prozerin JDMF during the approval evaluation for pharmaceutical products. At the time of Prozerin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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